Canonical Allele Identifier: CA1583158484

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1753226893

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419576_132419577del , CM000667.2:g.132419576_132419577del	GRCh38
NC_000005.9:g.131755268_131755269del , CM000667.1:g.131755268_131755269del	GRCh37
NC_000005.8:g.131783167_131783168del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-247_-326-246del	ENSP00000492349.2:n.-326-247_-326-246del
ENST00000638504.1:n.89-247_89-246del
ENST00000638568.2:c.-468-247_-468-246del	ENSP00000491158.2:n.-468-247_-468-246del
ENST00000639899.1:n.132-247_132-246del
ENST00000337752.6:c.-70-247_-70-246del (CARINH)	ENSP00000338228.2:n.-70-247_-70-246del
ENST00000378947.7:c.-70-247_-70-246del (CARINH)	ENSP00000368230.3:n.-70-247_-70-246del
ENST00000378953.8:c.-70-247_-70-246del (CARINH)	ENSP00000368236.4:n.-70-247_-70-246del
ENST00000407797.5:c.-70-247_-70-246del (CARINH)	ENSP00000385513.1:n.-70-247_-70-246del
ENST00000461203.5:n.62-247_62-246del (CARINH)
NR_045116.1:n.270-247_270-246del (CARINH)
NM_001207001.2:c.-70-247_-70-246del (CARINH)	NP_001193930.1:n.-70-247_-70-246del
XR_948788.3:n.1068_1069del (LINC02863)
NR_161242.1:n.114-247_114-246del (CARINH)