Canonical Allele Identifier: CA2611438364

Gene: MGMT

Linked Data

• gnomAD v4: 10-129767079-TAAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767080_129767083del , CM000672.2:g.129767080_129767083del	GRCh38
NC_000010.10:g.131565344_131565347del , CM000672.1:g.131565344_131565347del	GRCh37
NC_000010.9:g.131455334_131455337del	NCBI36
NG_052673.1:g.304897_304900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*83_*86del	ENSP00000302111.7:n.*83_*86del
ENST00000651593.1:c.*83_*86del MANE Select	ENSP00000498729.1:n.*83_*86del
ENST00000306010.7:c.*83_*86del	ENSP00000302111.7:n.*83_*86del
NM_002412.3:c.*83_*86del	NP_002403.2:n.*83_*86del
NM_002412.4:c.*83_*86del	NP_002403.2:n.*83_*86del
XM_005252682.2:c.*83_*86del	XP_005252739.1:n.*83_*86del
XM_006717863.2:c.*83_*86del	XP_006717926.1:n.*83_*86del
XM_011539817.1:c.*83_*86del	XP_011538119.1:n.*83_*86del
NM_002412.5:c.*83_*86del MANE Select	NP_002403.3:n.*83_*86del
XM_017016275.1:c.*83_*86del	XP_016871764.1:n.*83_*86del