Canonical Allele Identifier: CA2611438359

Gene: MGMT

Linked Data

• gnomAD v4: 10-129767073-CTGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767074_129767076del , CM000672.2:g.129767074_129767076del	GRCh38
NC_000010.10:g.131565338_131565340del , CM000672.1:g.131565338_131565340del	GRCh37
NC_000010.9:g.131455328_131455330del	NCBI36
NG_052673.1:g.304891_304893del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*77_*79del	ENSP00000302111.7:n.*77_*79del
ENST00000651593.1:c.*77_*79del MANE Select	ENSP00000498729.1:n.*77_*79del
ENST00000306010.7:c.*77_*79del	ENSP00000302111.7:n.*77_*79del
NM_002412.3:c.*77_*79del	NP_002403.2:n.*77_*79del
NM_002412.4:c.*77_*79del	NP_002403.2:n.*77_*79del
XM_005252682.2:c.*77_*79del	XP_005252739.1:n.*77_*79del
XM_006717863.2:c.*77_*79del	XP_006717926.1:n.*77_*79del
XM_011539817.1:c.*77_*79del	XP_011538119.1:n.*77_*79del
NM_002412.5:c.*77_*79del MANE Select	NP_002403.3:n.*77_*79del
XM_017016275.1:c.*77_*79del	XP_016871764.1:n.*77_*79del