Canonical Allele Identifier: CA2611438385

Gene: MGMT

Linked Data

• gnomAD v4: 10-129767110-G-GTGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767113_129767116dup , CM000672.2:g.129767113_129767116dup	GRCh38
NC_000010.10:g.131565377_131565380dup , CM000672.1:g.131565377_131565380dup	GRCh37
NC_000010.9:g.131455367_131455370dup	NCBI36
NG_052673.1:g.304930_304933dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*116_*119dup	ENSP00000302111.7:n.*116_*119dup
ENST00000651593.1:c.*116_*119dup MANE Select	ENSP00000498729.1:n.*116_*119dup
ENST00000306010.7:c.*116_*119dup	ENSP00000302111.7:n.*116_*119dup
NM_002412.3:c.*116_*119dup	NP_002403.2:n.*116_*119dup
NM_002412.4:c.*116_*119dup	NP_002403.2:n.*116_*119dup
XM_006717863.2:c.*116_*119dup	XP_006717926.1:n.*116_*119dup
XM_011539817.1:c.*116_*119dup	XP_011538119.1:n.*116_*119dup
NM_002412.5:c.*116_*119dup MANE Select	NP_002403.3:n.*116_*119dup
XM_017016275.1:c.*116_*119dup	XP_016871764.1:n.*116_*119dup