Canonical Allele Identifier: CA1583158616
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419874C= , CM000667.2:g.132419874C= GRCh38
NC_000005.9:g.131755566C= , CM000667.1:g.131755566C= GRCh37
NC_000005.8:g.131783465C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-275C= ENSP00000492349.2:n.-275C=
ENST00000638504.1:n.140C=
ENST00000638568.2:c.-417C= ENSP00000491158.2:n.-417C=
ENST00000639899.1:n.183C=
ENST00000337752.6:c.-19C= (CARINH) ENSP00000338228.2:n.-19C=
ENST00000378947.7:c.-19C= (CARINH) ENSP00000368230.3:n.-19C=
ENST00000378953.8:c.-19C= (CARINH) ENSP00000368236.4:n.-19C=
ENST00000407797.5:c.-19C= (CARINH) ENSP00000385513.1:n.-19C=
ENST00000461203.5:n.113C= (CARINH)
ENST00000621237.1:c.-19C= (CARINH) ENSP00000481774.1:n.-19C=
NR_045116.1:n.321C= (CARINH)
NM_001207001.2:c.-19C= (CARINH) NP_001193930.1:n.-19C=
XR_948788.3:n.894-125G= (LINC02863)
NR_161242.1:n.165C= (CARINH)