Canonical Allele Identifier: CA2675201343

Gene: CARINH LINC02863

Linked Data

• gnomAD v4: 5-132419507-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419509_132419510del , CM000667.2:g.132419509_132419510del	GRCh38
NC_000005.9:g.131755201_131755202del , CM000667.1:g.131755201_131755202del	GRCh37
NC_000005.8:g.131783100_131783101del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-314_-326-313del	ENSP00000492349.2:n.-326-314_-326-313del
ENST00000638504.1:n.89-314_89-313del
ENST00000638568.2:c.-468-314_-468-313del	ENSP00000491158.2:n.-468-314_-468-313del
ENST00000639899.1:n.132-314_132-313del
ENST00000337752.6:c.-70-314_-70-313del (CARINH)	ENSP00000338228.2:n.-70-314_-70-313del
ENST00000378947.7:c.-70-314_-70-313del (CARINH)	ENSP00000368230.3:n.-70-314_-70-313del
ENST00000378953.8:c.-70-314_-70-313del (CARINH)	ENSP00000368236.4:n.-70-314_-70-313del
ENST00000407797.5:c.-70-314_-70-313del (CARINH)	ENSP00000385513.1:n.-70-314_-70-313del
ENST00000461203.5:n.62-314_62-313del (CARINH)
NR_045116.1:n.270-314_270-313del (CARINH)
NM_001207001.2:c.-70-314_-70-313del (CARINH)	NP_001193930.1:n.-70-314_-70-313del
XR_948788.3:n.1134_1135del (LINC02863)
NR_161242.1:n.114-314_114-313del (CARINH)