Canonical Allele Identifier: CA1583158570
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

dbSNP Id: rs1753232858
gnomAD v4: 5-132419799-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419805del , CM000667.2:g.132419805del GRCh38
NC_000005.9:g.131755497del , CM000667.1:g.131755497del GRCh37
NC_000005.8:g.131783396del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-326-18del ENSP00000492349.2:n.-326-18del
ENST00000638504.1:n.89-18del
ENST00000638568.2:c.-468-18del ENSP00000491158.2:n.-468-18del
ENST00000639899.1:n.132-18del
ENST00000337752.6:c.-70-18del (CARINH) ENSP00000338228.2:n.-70-18del
ENST00000378947.7:c.-70-18del (CARINH) ENSP00000368230.3:n.-70-18del
ENST00000378953.8:c.-70-18del (CARINH) ENSP00000368236.4:n.-70-18del
ENST00000407797.5:c.-70-18del (CARINH) ENSP00000385513.1:n.-70-18del
ENST00000461203.5:n.62-18del (CARINH)
NR_045116.1:n.270-18del (CARINH)
NM_001207001.2:c.-70-18del (CARINH) NP_001193930.1:n.-70-18del
XR_948788.3:n.894-51del (LINC02863)
NR_161242.1:n.114-18del (CARINH)
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