Canonical Allele Identifier: CA378713276

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565226G>T (hg19) ; chr10:g.129766962G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766962G>T , CM000672.2:g.129766962G>T	GRCh38
NC_000010.10:g.131565226G>T , CM000672.1:g.131565226G>T	GRCh37
NC_000010.9:g.131455216G>T	NCBI36
NG_052673.1:g.304779G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.682G>T	ENSP00000302111.7:p.Ala228Ser
ENST00000651593.1:c.589G>T MANE Select	ENSP00000498729.1:p.Ala197Ser
ENST00000306010.7:c.682G>T	ENSP00000302111.7:p.Ala228Ser
NM_002412.3:c.682G>T	NP_002403.2:p.Ala228Ser
NM_002412.4:c.682G>T	NP_002403.2:p.Ala228Ser
XM_005252682.2:c.589G>T	XP_005252739.1:p.Ala197Ser
XM_006717863.2:c.412G>T	XP_006717926.1:p.Ala138Ser
XM_011539817.1:c.598G>T	XP_011538119.1:p.Ala200Ser
NM_002412.5:c.589G>T MANE Select	NP_002403.3:p.Ala197Ser
XM_017016275.1:c.412G>T	XP_016871764.1:p.Ala138Ser