Canonical Allele Identifier: CA1583158630

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419911G= , CM000667.2:g.132419911G=	GRCh38
NC_000005.9:g.131755603G= , CM000667.1:g.131755603G=	GRCh37
NC_000005.8:g.131783502G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-238G=	ENSP00000492349.2:n.-238G=
ENST00000638504.1:n.177G=
ENST00000638568.2:c.-380G=	ENSP00000491158.2:n.-380G=
ENST00000639899.1:n.220G=
ENST00000337752.6:c.19G= (CARINH)	ENSP00000338228.2:p.Gly7=
ENST00000378947.7:c.19G= (CARINH)	ENSP00000368230.3:p.Gly7=
ENST00000378953.8:c.19G= (CARINH)	ENSP00000368236.4:p.Gly7=
ENST00000407797.5:c.19G= (CARINH)	ENSP00000385513.1:p.Gly7=
ENST00000461203.5:n.150G= (CARINH)
ENST00000621237.1:c.19G= (CARINH)	ENSP00000481774.1:p.Gly7=
NR_045116.1:n.358G= (CARINH)
NM_001207001.2:c.19G= (CARINH)	NP_001193930.1:p.Gly7=
XR_948788.3:n.894-162C= (LINC02863)
NR_161242.1:n.202G= (CARINH)