Canonical Allele Identifier: CA886100511

Gene: MTHFR

Linked Data

• dbSNP Id: rs1368098297
• gnomAD v3: 1-11796094-TCTGGGAAGAA-T
• gnomAD v4: 1-11796094-TCTGGGAAGAA-T
• MyVariant Identifiers: chr1:g.11856152_11856161del (hg19) ; chr1:g.11796095_11796104del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11796097_11796106del , CM000663.2:g.11796097_11796106del	GRCh38
NC_000001.10:g.11856154_11856163del , CM000663.1:g.11856154_11856163del	GRCh37
NC_000001.9:g.11778741_11778750del	NCBI36
NG_013351.1:g.15000_15009del , LRG_726:g.15000_15009del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.903+102_903+111del	ENSP00000365770.1:n.903+102_903+111del
ENST00000376590.9:c.780+102_780+111del MANE Select	ENSP00000365775.3:n.780+102_780+111del
ENST00000376592.6:c.780+102_780+111del	ENSP00000365777.1:n.780+102_780+111del
ENST00000423400.7:c.900+102_900+111del	ENSP00000398908.3:n.900+102_900+111del
ENST00000641407.1:c.780+102_780+111del	ENSP00000493098.1:n.780+102_780+111del
ENST00000641446.1:c.780+102_780+111del	ENSP00000493262.1:n.780+102_780+111del
ENST00000641721.1:n.644-756_644-747del
ENST00000641747.1:c.*292+102_*292+111del	ENSP00000493116.1:n.*292+102_*292+111del
ENST00000641759.1:n.915+102_915+111del
ENST00000641805.1:n.1063+102_1063+111del
ENST00000641820.1:c.45+102_45+111del	ENSP00000492937.1:n.45+102_45+111del
ENST00000376583.7:c.903+102_903+111del	ENSP00000365767.3:n.903+102_903+111del
ENST00000376585.5:c.903+102_903+111del	ENSP00000365770.1:n.903+102_903+111del
ENST00000376590.7:c.780+102_780+111del	ENSP00000365775.3:n.780+102_780+111del
ENST00000376592.5:c.780+102_780+111del	ENSP00000365777.1:n.780+102_780+111del
NM_005957.4:c.780+102_780+111del , LRG_726t1:c.780+102_780+111del	NP_005948.3:n.780+102_780+111del
XM_005263458.2:c.903+102_903+111del	XP_005263515.1:n.903+102_903+111del
XM_005263460.3:c.780+102_780+111del	XP_005263517.1:n.780+102_780+111del
XM_005263461.3:c.780+102_780+111del	XP_005263518.1:n.780+102_780+111del
XM_005263462.3:c.780+102_780+111del	XP_005263519.1:n.780+102_780+111del
XM_005263463.2:c.534+102_534+111del	XP_005263520.1:n.534+102_534+111del
XM_011541495.1:c.900+102_900+111del	XP_011539797.1:n.900+102_900+111del
XM_011541496.1:c.903+102_903+111del	XP_011539798.1:n.903+102_903+111del
NM_001330358.1:c.903+102_903+111del	NP_001317287.1:n.903+102_903+111del
XM_005263460.5:c.780+102_780+111del	XP_005263517.1:n.780+102_780+111del
XM_005263462.4:c.780+102_780+111del	XP_005263519.1:n.780+102_780+111del
XM_005263463.4:c.534+102_534+111del	XP_005263520.1:n.534+102_534+111del
XM_011541495.3:c.900+102_900+111del	XP_011539797.1:n.900+102_900+111del
XM_011541496.3:c.903+102_903+111del	XP_011539798.1:n.903+102_903+111del
XM_017001328.2:c.903+102_903+111del	XP_016856817.1:n.903+102_903+111del
XM_024447198.1:c.534+102_534+111del	XP_024302966.1:n.534+102_534+111del
XR_002956640.1:n.1647+102_1647+111del
NM_005957.5:c.780+102_780+111del MANE Select	NP_005948.3:n.780+102_780+111del
NM_001330358.2:c.903+102_903+111del	NP_001317287.1:n.903+102_903+111del