Canonical Allele Identifier: CA378712984

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766816-T-C
• MyVariant Identifiers: chr10:g.131565080T>C (hg19) ; chr10:g.129766816T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766816T>C , CM000672.2:g.129766816T>C	GRCh38
NC_000010.10:g.131565080T>C , CM000672.1:g.131565080T>C	GRCh37
NC_000010.9:g.131455070T>C	NCBI36
NG_052673.1:g.304633T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.536T>C	ENSP00000302111.7:p.Val179Ala
ENST00000651593.1:c.443T>C MANE Select	ENSP00000498729.1:p.Val148Ala
ENST00000306010.7:c.536T>C	ENSP00000302111.7:p.Val179Ala
NM_002412.3:c.536T>C	NP_002403.2:p.Val179Ala
NM_002412.4:c.536T>C	NP_002403.2:p.Val179Ala
XM_005252682.2:c.443T>C	XP_005252739.1:p.Val148Ala
XM_006717863.2:c.266T>C	XP_006717926.1:p.Val89Ala
XM_011539817.1:c.452T>C	XP_011538119.1:p.Val151Ala
NM_002412.5:c.443T>C MANE Select	NP_002403.3:p.Val148Ala
XM_017016275.1:c.266T>C	XP_016871764.1:p.Val89Ala