Canonical Allele Identifier: CA351976698

Gene: CMTM7

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32391961G>A , CM000665.2:g.32391961G>A	GRCh38
NC_000003.11:g.32433453G>A , CM000665.1:g.32433453G>A	GRCh37
NC_000003.10:g.32408457G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_138410.4:c.55G>A MANE Select	NP_612419.1:p.Gly19Arg
ENST00000334983.10:c.55G>A MANE Select	ENSP00000335605.5:p.Gly19Arg
NM_138410.2:c.55G>A	NP_612419.1:p.Gly19Arg
NM_138410.3:c.55G>A	NP_612419.1:p.Gly19Arg
NM_181472.1:c.55G>A	NP_852137.1:p.Gly19Arg
NM_181472.2:c.55G>A	NP_852137.1:p.Gly19Arg
NM_181472.3:c.55G>A	NP_852137.1:p.Gly19Arg
ENST00000334983.9:c.55G>A	ENSP00000335605.5:p.Gly19Arg
ENST00000349718.8:c.55G>A	ENSP00000283621.5:p.Gly19Arg
ENST00000454304.6:c.55G>A	ENSP00000414480.2:p.Gly19Arg
XM_011533319.1:c.55G>A	XP_011531621.1:p.Gly19Arg
XM_011533319.2:c.55G>A	XP_011531621.1:p.Gly19Arg
XM_017005646.1:c.55G>A	XP_016861135.1:p.Gly19Arg