Canonical Allele Identifier: CA1583158623
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419897A= , CM000667.2:g.132419897A= GRCh38
NC_000005.9:g.131755589A= , CM000667.1:g.131755589A= GRCh37
NC_000005.8:g.131783488A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-252A= ENSP00000492349.2:n.-252A=
ENST00000638504.1:n.163A=
ENST00000638568.2:c.-394A= ENSP00000491158.2:n.-394A=
ENST00000639899.1:n.206A=
ENST00000337752.6:c.5A= (CARINH) ENSP00000338228.2:p.Asp2=
ENST00000378947.7:c.5A= (CARINH) ENSP00000368230.3:p.Asp2=
ENST00000378953.8:c.5A= (CARINH) ENSP00000368236.4:p.Asp2=
ENST00000407797.5:c.5A= (CARINH) ENSP00000385513.1:p.Asp2=
ENST00000461203.5:n.136A= (CARINH)
ENST00000621237.1:c.5A= (CARINH) ENSP00000481774.1:p.Asp2=
NR_045116.1:n.344A= (CARINH)
NM_001207001.2:c.5A= (CARINH) NP_001193930.1:p.Asp2=
XR_948788.3:n.894-148T= (LINC02863)
NR_161242.1:n.188A= (CARINH)