Canonical Allele Identifier: CA1583158637
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419923G= , CM000667.2:g.132419923G= GRCh38
NC_000005.9:g.131755615G= , CM000667.1:g.131755615G= GRCh37
NC_000005.8:g.131783514G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-226G= ENSP00000492349.2:n.-226G=
ENST00000638504.1:n.189G=
ENST00000638568.2:c.-368G= ENSP00000491158.2:n.-368G=
ENST00000639899.1:n.232G=
ENST00000337752.6:c.31G= (CARINH) ENSP00000338228.2:p.Ala11=
ENST00000378947.7:c.31G= (CARINH) ENSP00000368230.3:p.Ala11=
ENST00000378953.8:c.31G= (CARINH) ENSP00000368236.4:p.Ala11=
ENST00000407797.5:c.31G= (CARINH) ENSP00000385513.1:p.Ala11=
ENST00000461203.5:n.162G= (CARINH)
ENST00000621237.1:c.31G= (CARINH) ENSP00000481774.1:p.Ala11=
NR_045116.1:n.370G= (CARINH)
NM_001207001.2:c.31G= (CARINH) NP_001193930.1:p.Ala11=
XR_948788.3:n.894-174C= (LINC02863)
NR_161242.1:n.214G= (CARINH)