Canonical Allele Identifier: CA1583158628
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419910_132419911delinsTG , CM000667.2:g.132419910_132419911delinsTG GRCh38
NC_000005.9:g.131755602_131755603delinsTG , CM000667.1:g.131755602_131755603delinsTG GRCh37
NC_000005.8:g.131783501_131783502delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-239_-238delinsTG ENSP00000492349.2:n.-239_-238delinsTG
ENST00000638504.1:n.176_177delinsTG
ENST00000638568.2:c.-381_-380delinsTG ENSP00000491158.2:n.-381_-380delinsTG
ENST00000639899.1:n.219_220delinsTG
ENST00000337752.6:c.18_19delinsTG (CARINH) ENSP00000338228.2:p.Ala6=
ENST00000378947.7:c.18_19delinsTG (CARINH) ENSP00000368230.3:p.Ala6=
ENST00000378953.8:c.18_19delinsTG (CARINH) ENSP00000368236.4:p.Ala6=
ENST00000407797.5:c.18_19delinsTG (CARINH) ENSP00000385513.1:p.Ala6=
ENST00000461203.5:n.149_150delinsTG (CARINH)
ENST00000621237.1:c.18_19delinsTG (CARINH) ENSP00000481774.1:p.Ala6=
NR_045116.1:n.357_358delinsTG (CARINH)
NM_001207001.2:c.18_19delinsTG (CARINH) NP_001193930.1:p.Ala6=
XR_948788.3:n.894-162_894-161delinsCA (LINC02863)
NR_161242.1:n.201_202delinsTG (CARINH)