Canonical Allele Identifier: CA1583158627

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419906C= , CM000667.2:g.132419906C=	GRCh38
NC_000005.9:g.131755598C= , CM000667.1:g.131755598C=	GRCh37
NC_000005.8:g.131783497C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-243C=	ENSP00000492349.2:n.-243C=
ENST00000638504.1:n.172C=
ENST00000638568.2:c.-385C=	ENSP00000491158.2:n.-385C=
ENST00000639899.1:n.215C=
ENST00000337752.6:c.14C= (CARINH)	ENSP00000338228.2:p.Ala5=
ENST00000378947.7:c.14C= (CARINH)	ENSP00000368230.3:p.Ala5=
ENST00000378953.8:c.14C= (CARINH)	ENSP00000368236.4:p.Ala5=
ENST00000407797.5:c.14C= (CARINH)	ENSP00000385513.1:p.Ala5=
ENST00000461203.5:n.145C= (CARINH)
ENST00000621237.1:c.14C= (CARINH)	ENSP00000481774.1:p.Ala5=
NR_045116.1:n.353C= (CARINH)
NM_001207001.2:c.14C= (CARINH)	NP_001193930.1:p.Ala5=
XR_948788.3:n.894-157G= (LINC02863)
NR_161242.1:n.197C= (CARINH)