Canonical Allele Identifier: CA378712969

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565074A>C (hg19) ; chr10:g.129766810A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766810A>C , CM000672.2:g.129766810A>C	GRCh38
NC_000010.10:g.131565074A>C , CM000672.1:g.131565074A>C	GRCh37
NC_000010.9:g.131455064A>C	NCBI36
NG_052673.1:g.304627A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000306010.8:c.530A>C	ENSP00000302111.7:p.His177Pro
ENST00000651593.1:c.437A>C MANE Select	ENSP00000498729.1:p.His146Pro
ENST00000306010.7:c.530A>C	ENSP00000302111.7:p.His177Pro
NM_002412.3:c.530A>C	NP_002403.2:p.His177Pro
NM_002412.4:c.530A>C	NP_002403.2:p.His177Pro
XM_005252682.2:c.437A>C	XP_005252739.1:p.His146Pro
XM_006717863.2:c.260A>C	XP_006717926.1:p.His87Pro
XM_011539817.1:c.446A>C	XP_011538119.1:p.His149Pro
NM_002412.5:c.437A>C MANE Select	NP_002403.3:p.His146Pro
XM_017016275.1:c.260A>C	XP_016871764.1:p.His87Pro