Canonical Allele Identifier: CA1583158593
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419836C= , CM000667.2:g.132419836C= GRCh38
NC_000005.9:g.131755528C= , CM000667.1:g.131755528C= GRCh37
NC_000005.8:g.131783427C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-313C= ENSP00000492349.2:n.-313C=
ENST00000638504.1:n.102C=
ENST00000638568.2:c.-455C= ENSP00000491158.2:n.-455C=
ENST00000639899.1:n.145C=
ENST00000337752.6:c.-57C= (CARINH) ENSP00000338228.2:n.-57C=
ENST00000378947.7:c.-57C= (CARINH) ENSP00000368230.3:n.-57C=
ENST00000378953.8:c.-57C= (CARINH) ENSP00000368236.4:n.-57C=
ENST00000407797.5:c.-57C= (CARINH) ENSP00000385513.1:n.-57C=
ENST00000461203.5:n.75C= (CARINH)
NR_045116.1:n.283C= (CARINH)
NM_001207001.2:c.-57C= (CARINH) NP_001193930.1:n.-57C=
XR_948788.3:n.894-87G= (LINC02863)
NR_161242.1:n.127C= (CARINH)