Canonical Allele Identifier: CA446357994
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.131755599T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419907T>A , CM000667.2:g.132419907T>A GRCh38
NC_000005.9:g.131755599T>A , CM000667.1:g.131755599T>A GRCh37
NC_000005.8:g.131783498T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-242T>A ENSP00000492349.2:n.-242T>A
ENST00000638504.1:n.173T>A
ENST00000638568.2:c.-384T>A ENSP00000491158.2:n.-384T>A
ENST00000639899.1:n.216T>A
ENST00000337752.6:c.15T>A (CARINH) ENSP00000338228.2:p.Ala5=
ENST00000378947.7:c.15T>A (CARINH) ENSP00000368230.3:p.Ala5=
ENST00000378953.8:c.15T>A (CARINH) ENSP00000368236.4:p.Ala5=
ENST00000407797.5:c.15T>A (CARINH) ENSP00000385513.1:p.Ala5=
ENST00000461203.5:n.146T>A (CARINH)
ENST00000621237.1:c.15T>A (CARINH) ENSP00000481774.1:p.Ala5=
NR_045116.1:n.354T>A (CARINH)
NM_001207001.2:c.15T>A (CARINH) NP_001193930.1:p.Ala5=
XR_948788.3:n.894-158A>T (LINC02863)
NR_161242.1:n.198T>A (CARINH)