Canonical Allele Identifier: CA7693108

Gene: CEMIP

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80920267G>A , CM000677.2:g.80920267G>A	GRCh38
NC_000015.9:g.81212608G>A , CM000677.1:g.81212608G>A	GRCh37
NC_000015.8:g.78999663G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394685.8:c.1971G>A MANE Select	ENSP00000378177.3:p.Pro657=
ENST00000220244.7:c.1971G>A	ENSP00000220244.3:p.Pro657=
ENST00000356249.9:c.1971G>A	ENSP00000348583.5:p.Pro657=
ENST00000394685.7:c.1971G>A	ENSP00000378177.3:p.Pro657=
ENST00000611615.1:c.1971G>A	ENSP00000480324.1:p.Pro657=
NM_001293298.1:c.1971G>A	NP_001280227.1:p.Pro657=
NM_001293304.1:c.1971G>A	NP_001280233.1:p.Pro657=
NM_018689.2:c.1971G>A	NP_061159.1:p.Pro657=
XM_024450001.1:c.2076G>A	XP_024305769.1:p.Pro692=
NM_001293298.2:c.1971G>A MANE Select	NP_001280227.1:p.Pro657=
NM_001293304.2:c.1971G>A	NP_001280233.1:p.Pro657=
NM_018689.3:c.1971G>A	NP_061159.1:p.Pro657=