Canonical Allele Identifier: CA906302248

Gene: CMTM7

Linked Data

• dbSNP Id: rs12638540
• gnomAD v3: 3-32447042-A-T
• gnomAD v4: 3-32447042-A-T
• MyVariant Identifiers: chr3:g.32488534A>T (hg19) ; chr3:g.32447042A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32447042A>T , CM000665.2:g.32447042A>T	GRCh38
NC_000003.11:g.32488534A>T , CM000665.1:g.32488534A>T	GRCh37
NC_000003.10:g.32463538A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000334983.10:c.334-2412A>T MANE Select	ENSP00000335605.5:n.334-2412A>T
ENST00000334983.9:c.334-2412A>T	ENSP00000335605.5:n.334-2412A>T
ENST00000349718.8:c.333+5029A>T	ENSP00000283621.5:n.333+5029A>T
ENST00000454304.6:c.334-2412A>T	ENSP00000414480.2:n.334-2412A>T
ENST00000465248.1:c.201+5029A>T	ENSP00000440333.1:n.201+5029A>T
NM_138410.2:c.334-2412A>T	NP_612419.1:n.334-2412A>T
NM_181472.1:c.333+5029A>T	NP_852137.1:n.333+5029A>T
XM_011533319.1:c.334-2412A>T	XP_011531621.1:n.334-2412A>T
NM_138410.3:c.334-2412A>T	NP_612419.1:n.334-2412A>T
NM_181472.2:c.333+5029A>T	NP_852137.1:n.333+5029A>T
XM_011533319.2:c.334-2412A>T	XP_011531621.1:n.334-2412A>T
XM_017005646.1:c.334-2412A>T	XP_016861135.1:n.334-2412A>T
NM_138410.4:c.334-2412A>T MANE Select	NP_612419.1:n.334-2412A>T
NM_181472.3:c.333+5029A>T	NP_852137.1:n.333+5029A>T