Canonical Allele Identifier: CA471816466

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766817-G-T
• COSMIC: COSM6190765 ; COSM6190766
• MyVariant Identifiers: chr10:g.131565081G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766817G>T , CM000672.2:g.129766817G>T	GRCh38
NC_000010.10:g.131565081G>T , CM000672.1:g.131565081G>T	GRCh37
NC_000010.9:g.131455071G>T	NCBI36
NG_052673.1:g.304634G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.537G>T	ENSP00000302111.7:p.Val179=
ENST00000651593.1:c.444G>T MANE Select	ENSP00000498729.1:p.Val148=
ENST00000306010.7:c.537G>T	ENSP00000302111.7:p.Val179=
NM_002412.3:c.537G>T	NP_002403.2:p.Val179=
NM_002412.4:c.537G>T	NP_002403.2:p.Val179=
XM_005252682.2:c.444G>T	XP_005252739.1:p.Val148=
XM_006717863.2:c.267G>T	XP_006717926.1:p.Val89=
XM_011539817.1:c.453G>T	XP_011538119.1:p.Val151=
NM_002412.5:c.444G>T MANE Select	NP_002403.3:p.Val148=
XM_017016275.1:c.267G>T	XP_016871764.1:p.Val89=