Canonical Allele Identifier: CA1583158606
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419853C= , CM000667.2:g.132419853C= GRCh38
NC_000005.9:g.131755545C= , CM000667.1:g.131755545C= GRCh37
NC_000005.8:g.131783444C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-296C= ENSP00000492349.2:n.-296C=
ENST00000638504.1:n.119C=
ENST00000638568.2:c.-438C= ENSP00000491158.2:n.-438C=
ENST00000639899.1:n.162C=
ENST00000337752.6:c.-40C= (CARINH) ENSP00000338228.2:n.-40C=
ENST00000378947.7:c.-40C= (CARINH) ENSP00000368230.3:n.-40C=
ENST00000378953.8:c.-40C= (CARINH) ENSP00000368236.4:n.-40C=
ENST00000407797.5:c.-40C= (CARINH) ENSP00000385513.1:n.-40C=
ENST00000461203.5:n.92C= (CARINH)
NR_045116.1:n.300C= (CARINH)
NM_001207001.2:c.-40C= (CARINH) NP_001193930.1:n.-40C=
XR_948788.3:n.894-104G= (LINC02863)
NR_161242.1:n.144C= (CARINH)