Canonical Allele Identifier: CA2542446348

Gene: CMTM7

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32446968T>C , CM000665.2:g.32446968T>C	GRCh38
NC_000003.11:g.32488460T>C , CM000665.1:g.32488460T>C	GRCh37
NC_000003.10:g.32463464T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000334983.10:c.334-2486T>C MANE Select	ENSP00000335605.5:n.334-2486T>C
ENST00000334983.9:c.334-2486T>C	ENSP00000335605.5:n.334-2486T>C
ENST00000349718.8:c.333+4955T>C	ENSP00000283621.5:n.333+4955T>C
ENST00000454304.6:c.334-2486T>C	ENSP00000414480.2:n.334-2486T>C
ENST00000465248.1:c.201+4955T>C	ENSP00000440333.1:n.201+4955T>C
NM_138410.2:c.334-2486T>C	NP_612419.1:n.334-2486T>C
NM_181472.1:c.333+4955T>C	NP_852137.1:n.333+4955T>C
XM_011533319.1:c.334-2486T>C	XP_011531621.1:n.334-2486T>C
NM_138410.3:c.334-2486T>C	NP_612419.1:n.334-2486T>C
NM_181472.2:c.333+4955T>C	NP_852137.1:n.333+4955T>C
XM_011533319.2:c.334-2486T>C	XP_011531621.1:n.334-2486T>C
XM_017005646.1:c.334-2486T>C	XP_016861135.1:n.334-2486T>C
NM_138410.4:c.334-2486T>C MANE Select	NP_612419.1:n.334-2486T>C
NM_181472.3:c.333+4955T>C	NP_852137.1:n.333+4955T>C