Canonical Allele Identifier: CA11992463

Gene: MGAT1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180799673A>C , CM000667.2:g.180799673A>C	GRCh38
NC_000005.9:g.180226673A>C , CM000667.1:g.180226673A>C	GRCh37
NC_000005.8:g.180159279A>C	NCBI36
NG_032928.1:g.15465T>G
NG_032928.2:g.20980T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307826.5:c.-127+3007T>G MANE Select	ENSP00000311888.4:n.-127+3007T>G
ENST00000307826.4:c.-127+3007T>G	ENSP00000311888.4:n.-127+3007T>G
ENST00000333055.8:c.-126-6576T>G	ENSP00000332073.3:n.-126-6576T>G
ENST00000393340.7:c.-126-6576T>G	ENSP00000377010.3:n.-126-6576T>G
ENST00000427865.2:c.-127+3929T>G	ENSP00000402838.2:n.-127+3929T>G
ENST00000446023.6:c.-126-6576T>G	ENSP00000404718.2:n.-126-6576T>G
ENST00000502678.1:c.-126-6576T>G	ENSP00000422588.1:n.-126-6576T>G
ENST00000504385.5:n.505-6576T>G
ENST00000504671.1:c.-165+3007T>G	ENSP00000424891.1:n.-165+3007T>G
ENST00000505682.1:n.88+3007T>G
ENST00000506269.1:c.-127+3623T>G	ENSP00000422906.1:n.-127+3623T>G
ENST00000506889.1:c.-126-6576T>G	ENSP00000425988.1:n.-126-6576T>G
ENST00000507384.1:c.-347+3007T>G	ENSP00000427433.1:n.-347+3007T>G
ENST00000512695.1:c.-127+3733T>G	ENSP00000427116.1:n.-127+3733T>G
ENST00000513431.5:c.-126-6576T>G	ENSP00000423401.1:n.-126-6576T>G
ENST00000514283.1:c.-127+4140T>G	ENSP00000424382.1:n.-127+4140T>G
ENST00000514438.1:c.-126-6576T>G	ENSP00000421738.1:n.-126-6576T>G
ENST00000514760.1:n.144-3798T>G
NM_001114617.1:c.-126-6576T>G	NP_001108089.1:n.-126-6576T>G
NM_001114618.1:c.-126-6576T>G	NP_001108090.1:n.-126-6576T>G
NM_001114619.1:c.-127+4140T>G	NP_001108091.1:n.-127+4140T>G
NM_001114620.1:c.-127+3929T>G	NP_001108092.1:n.-127+3929T>G
NM_002406.3:c.-127+3007T>G	NP_002397.2:n.-127+3007T>G
XM_005265915.1:c.-126-6576T>G	XP_005265972.1:n.-126-6576T>G
XM_005265916.1:c.-126-6576T>G	XP_005265973.1:n.-126-6576T>G
XM_006714866.1:c.-126-6576T>G	XP_006714929.1:n.-126-6576T>G
XM_011534559.1:c.-126-6576T>G	XP_011532861.1:n.-126-6576T>G
XM_011534560.1:c.-126-6576T>G	XP_011532862.1:n.-126-6576T>G
XM_011534561.1:c.-126-6576T>G	XP_011532863.1:n.-126-6576T>G
XM_011534562.1:c.-126-6576T>G	XP_011532864.1:n.-126-6576T>G
XM_011534563.1:c.-126-6576T>G	XP_011532865.1:n.-126-6576T>G
NM_001364377.1:c.-126-6576T>G	NP_001351306.1:n.-126-6576T>G
NM_001364379.1:c.-126-6576T>G	NP_001351308.1:n.-126-6576T>G
NM_001364380.1:c.-126-6576T>G	NP_001351309.1:n.-126-6576T>G
NM_001364381.1:c.-126-6576T>G	NP_001351310.1:n.-126-6576T>G
NM_001364382.1:c.-126-6576T>G	NP_001351311.1:n.-126-6576T>G
NM_001364383.1:c.-126-6576T>G	NP_001351312.1:n.-126-6576T>G
NM_001364384.1:c.-126-6576T>G	NP_001351313.1:n.-126-6576T>G
NM_001364385.1:c.-126-6576T>G	NP_001351314.1:n.-126-6576T>G
NM_001364386.1:c.-126-6576T>G	NP_001351315.1:n.-126-6576T>G
NM_001364387.1:c.-126-6576T>G	NP_001351316.1:n.-126-6576T>G
NM_001364388.1:c.-126-6576T>G	NP_001351317.1:n.-126-6576T>G
NM_001364389.1:c.-127+3733T>G	NP_001351318.1:n.-127+3733T>G
NM_001364390.1:c.-127+3623T>G	NP_001351319.1:n.-127+3623T>G
NM_001364391.1:c.-144+3007T>G	NP_001351320.1:n.-144+3007T>G
NM_001364392.1:c.-127+3003T>G	NP_001351321.1:n.-127+3003T>G
NM_001364393.1:c.-227+3007T>G	NP_001351322.1:n.-227+3007T>G
NM_001364394.1:c.-347+3007T>G	NP_001351323.1:n.-347+3007T>G
NM_001364395.1:c.-165+3007T>G	NP_001351324.1:n.-165+3007T>G
NR_157150.1:n.193-3798T>G
NR_157151.1:n.672-3798T>G
NR_157152.1:n.1088-3798T>G
NR_157153.1:n.942-3798T>G
NR_157154.1:n.127+3007T>G
NM_001364377.2:c.-126-6576T>G	NP_001351306.1:n.-126-6576T>G
NM_001364379.2:c.-126-6576T>G	NP_001351308.1:n.-126-6576T>G
NM_001364380.2:c.-126-6576T>G	NP_001351309.1:n.-126-6576T>G
NM_001364381.2:c.-126-6576T>G	NP_001351310.1:n.-126-6576T>G
NM_001364382.2:c.-126-6576T>G	NP_001351311.1:n.-126-6576T>G
NM_001364383.2:c.-126-6576T>G	NP_001351312.1:n.-126-6576T>G
NM_001364384.2:c.-126-6576T>G	NP_001351313.1:n.-126-6576T>G
NM_001364385.2:c.-126-6576T>G	NP_001351314.1:n.-126-6576T>G
NM_001364386.2:c.-126-6576T>G	NP_001351315.1:n.-126-6576T>G
NM_001364387.2:c.-126-6576T>G	NP_001351316.1:n.-126-6576T>G
NM_001364388.2:c.-126-6576T>G	NP_001351317.1:n.-126-6576T>G
NM_001364389.2:c.-127+3733T>G	NP_001351318.1:n.-127+3733T>G
NM_001364390.2:c.-127+3623T>G	NP_001351319.1:n.-127+3623T>G
NM_001364391.2:c.-144+3007T>G	NP_001351320.1:n.-144+3007T>G
NM_001364392.2:c.-127+3003T>G	NP_001351321.1:n.-127+3003T>G
NM_001364393.2:c.-227+3007T>G	NP_001351322.1:n.-227+3007T>G
NM_001364394.2:c.-347+3007T>G	NP_001351323.1:n.-347+3007T>G
NM_001364395.2:c.-165+3007T>G	NP_001351324.1:n.-165+3007T>G
NM_002406.4:c.-127+3007T>G MANE Select	NP_002397.2:n.-127+3007T>G
NR_157150.2:n.193-3798T>G
NR_157151.2:n.672-3798T>G
NR_157152.2:n.1088-3798T>G
NR_157153.2:n.942-3798T>G
NR_157154.2:n.127+3007T>G
NM_001114617.2:c.-126-6576T>G	NP_001108089.1:n.-126-6576T>G