Canonical Allele Identifier: CA378713237

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766942-C-T
• MyVariant Identifiers: chr10:g.131565206C>T (hg19) ; chr10:g.129766942C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766942C>T , CM000672.2:g.129766942C>T	GRCh38
NC_000010.10:g.131565206C>T , CM000672.1:g.131565206C>T	GRCh37
NC_000010.9:g.131455196C>T	NCBI36
NG_052673.1:g.304759C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.662C>T	ENSP00000302111.7:p.Ala221Val
ENST00000651593.1:c.569C>T MANE Select	ENSP00000498729.1:p.Ala190Val
ENST00000306010.7:c.662C>T	ENSP00000302111.7:p.Ala221Val
NM_002412.3:c.662C>T	NP_002403.2:p.Ala221Val
NM_002412.4:c.662C>T	NP_002403.2:p.Ala221Val
XM_005252682.2:c.569C>T	XP_005252739.1:p.Ala190Val
XM_006717863.2:c.392C>T	XP_006717926.1:p.Ala131Val
XM_011539817.1:c.578C>T	XP_011538119.1:p.Ala193Val
NM_002412.5:c.569C>T MANE Select	NP_002403.3:p.Ala190Val
XM_017016275.1:c.392C>T	XP_016871764.1:p.Ala131Val