Canonical Allele Identifier: CA378713301

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766977-C-A
• MyVariant Identifiers: chr10:g.131565241C>A (hg19) ; chr10:g.129766977C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766977C>A , CM000672.2:g.129766977C>A	GRCh38
NC_000010.10:g.131565241C>A , CM000672.1:g.131565241C>A	GRCh37
NC_000010.9:g.131455231C>A	NCBI36
NG_052673.1:g.304794C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.697C>A	ENSP00000302111.7:p.Pro233Thr
ENST00000651593.1:c.604C>A MANE Select	ENSP00000498729.1:p.Pro202Thr
ENST00000306010.7:c.697C>A	ENSP00000302111.7:p.Pro233Thr
NM_002412.3:c.697C>A	NP_002403.2:p.Pro233Thr
NM_002412.4:c.697C>A	NP_002403.2:p.Pro233Thr
XM_005252682.2:c.604C>A	XP_005252739.1:p.Pro202Thr
XM_006717863.2:c.427C>A	XP_006717926.1:p.Pro143Thr
XM_011539817.1:c.613C>A	XP_011538119.1:p.Pro205Thr
NM_002412.5:c.604C>A MANE Select	NP_002403.3:p.Pro202Thr
XM_017016275.1:c.427C>A	XP_016871764.1:p.Pro143Thr