Canonical Allele Identifier: CA2611438356

Gene: MGMT

Linked Data

• gnomAD v4: 10-129767072-G-GCATC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767073_129767074insATCC , CM000672.2:g.129767073_129767074insATCC	GRCh38
NC_000010.10:g.131565337_131565338insATCC , CM000672.1:g.131565337_131565338insATCC	GRCh37
NC_000010.9:g.131455327_131455328insATCC	NCBI36
NG_052673.1:g.304890_304891insATCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*76_*77insATCC	ENSP00000302111.7:n.*76_*77insATCC
ENST00000651593.1:c.*76_*77insATCC MANE Select	ENSP00000498729.1:n.*76_*77insATCC
ENST00000306010.7:c.*76_*77insATCC	ENSP00000302111.7:n.*76_*77insATCC
NM_002412.3:c.*76_*77insATCC	NP_002403.2:n.*76_*77insATCC
NM_002412.4:c.*76_*77insATCC	NP_002403.2:n.*76_*77insATCC
XM_005252682.2:c.*76_*77insATCC	XP_005252739.1:n.*76_*77insATCC
XM_006717863.2:c.*76_*77insATCC	XP_006717926.1:n.*76_*77insATCC
XM_011539817.1:c.*76_*77insATCC	XP_011538119.1:n.*76_*77insATCC
NM_002412.5:c.*76_*77insATCC MANE Select	NP_002403.3:n.*76_*77insATCC
XM_017016275.1:c.*76_*77insATCC	XP_016871764.1:n.*76_*77insATCC