Canonical Allele Identifier: CA1583158638
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419928C= , CM000667.2:g.132419928C= GRCh38
NC_000005.9:g.131755620C= , CM000667.1:g.131755620C= GRCh37
NC_000005.8:g.131783519C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-221C= ENSP00000492349.2:n.-221C=
ENST00000638504.1:n.194C=
ENST00000638568.2:c.-363C= ENSP00000491158.2:n.-363C=
ENST00000639899.1:n.237C=
ENST00000337752.6:c.36C= (CARINH) ENSP00000338228.2:p.Ser12=
ENST00000378947.7:c.36C= (CARINH) ENSP00000368230.3:p.Ser12=
ENST00000378953.8:c.36C= (CARINH) ENSP00000368236.4:p.Ser12=
ENST00000407797.5:c.36C= (CARINH) ENSP00000385513.1:p.Ser12=
ENST00000461203.5:n.167C= (CARINH)
ENST00000621237.1:c.36C= (CARINH) ENSP00000481774.1:p.Ser12=
NR_045116.1:n.375C= (CARINH)
NM_001207001.2:c.36C= (CARINH) NP_001193930.1:p.Ser12=
XR_948788.3:n.894-179G= (LINC02863)
NR_161242.1:n.219C= (CARINH)