Canonical Allele Identifier: CA437092535

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182755157A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037369A>C , CM000665.2:g.183037369A>C	GRCh38
NC_000003.11:g.182755157A>C , CM000665.1:g.182755157A>C	GRCh37
NC_000003.10:g.184237851A>C	NCBI36
NG_008100.1:g.67209T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1443T>G MANE Select	ENSP00000265594.4:p.Ala481=
ENST00000265594.8:c.1443T>G	ENSP00000265594.4:p.Ala481=
ENST00000476176.5:c.1302T>G	ENSP00000420433.1:p.Ala434=
ENST00000492597.5:c.1116T>G	ENSP00000419898.1:p.Ala372=
ENST00000495767.5:c.*1024T>G	ENSP00000419658.1:n.*1024T>G
ENST00000497830.5:c.*1040T>G	ENSP00000420088.1:n.*1040T>G
ENST00000497959.5:c.1263+1657T>G	ENSP00000420648.1:n.1263+1657T>G
ENST00000539926.5:c.993T>G	ENSP00000441253.2:p.Ala331=
ENST00000610757.4:c.993T>G	ENSP00000480435.1:p.Ala331=
ENST00000629669.2:c.1263+1657T>G	ENSP00000486824.1:n.1263+1657T>G
NM_001293273.1:c.1092T>G	NP_001280202.1:p.Ala364=
NM_020166.4:c.1443T>G	NP_064551.3:p.Ala481=
NR_120639.1:n.1357T>G
NR_120640.1:n.2044+1657T>G
XM_006713702.1:c.1116T>G	XP_006713765.1:p.Ala372=
XM_011512992.1:c.1329T>G	XP_011511294.1:p.Ala443=
XM_011512993.1:c.1377+1657T>G	XP_011511295.1:n.1377+1657T>G
XR_241502.2:n.1524+1657T>G
XR_924159.1:n.1590T>G
NM_001363880.1:c.1116T>G	NP_001350809.1:p.Ala372=
XM_011512992.2:c.1329T>G	XP_011511294.1:p.Ala443=
XR_001740207.2:n.1566T>G
XR_001740208.2:n.1566T>G
XR_001740209.2:n.1470+1657T>G
XR_001740210.1:n.1396T>G
XR_002959553.1:n.1566T>G
XR_002959554.1:n.1500+1657T>G
XR_241502.3:n.1470+1657T>G
NM_020166.5:c.1443T>G MANE Select	NP_064551.3:p.Ala481=
NM_001293273.2:c.1092T>G	NP_001280202.1:p.Ala364=
NR_120639.2:n.1266T>G
NR_120640.2:n.2044+1657T>G