Canonical Allele Identifier: CA378712995

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565086G>A (hg19) ; chr10:g.129766822G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766822G>A , CM000672.2:g.129766822G>A	GRCh38
NC_000010.10:g.131565086G>A , CM000672.1:g.131565086G>A	GRCh37
NC_000010.9:g.131455076G>A	NCBI36
NG_052673.1:g.304639G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.542G>A	ENSP00000302111.7:p.Cys181Tyr
ENST00000651593.1:c.449G>A MANE Select	ENSP00000498729.1:p.Cys150Tyr
ENST00000306010.7:c.542G>A	ENSP00000302111.7:p.Cys181Tyr
NM_002412.3:c.542G>A	NP_002403.2:p.Cys181Tyr
NM_002412.4:c.542G>A	NP_002403.2:p.Cys181Tyr
XM_005252682.2:c.449G>A	XP_005252739.1:p.Cys150Tyr
XM_006717863.2:c.272G>A	XP_006717926.1:p.Cys91Tyr
XM_011539817.1:c.458G>A	XP_011538119.1:p.Cys153Tyr
NM_002412.5:c.449G>A MANE Select	NP_002403.3:p.Cys150Tyr
XM_017016275.1:c.272G>A	XP_016871764.1:p.Cys91Tyr