Canonical Allele Identifier: CA1583158466

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419500G= , CM000667.2:g.132419500G=	GRCh38
NC_000005.9:g.131755192G= , CM000667.1:g.131755192G=	GRCh37
NC_000005.8:g.131783091G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-323G=	ENSP00000492349.2:n.-326-323G=
ENST00000638504.1:n.89-323G=
ENST00000638568.2:c.-468-323G=	ENSP00000491158.2:n.-468-323G=
ENST00000639899.1:n.132-323G=
ENST00000337752.6:c.-70-323G= (CARINH)	ENSP00000338228.2:n.-70-323G=
ENST00000378947.7:c.-70-323G= (CARINH)	ENSP00000368230.3:n.-70-323G=
ENST00000378953.8:c.-70-323G= (CARINH)	ENSP00000368236.4:n.-70-323G=
ENST00000407797.5:c.-70-323G= (CARINH)	ENSP00000385513.1:n.-70-323G=
ENST00000461203.5:n.62-323G= (CARINH)
NR_045116.1:n.270-323G= (CARINH)
NM_001207001.2:c.-70-323G= (CARINH)	NP_001193930.1:n.-70-323G=
XR_948788.3:n.1143C= (LINC02863)
NR_161242.1:n.114-323G= (CARINH)