Canonical Allele Identifier: CA2675201305

Gene: CARINH LINC02863

Linked Data

• gnomAD v4: 5-132419433-ATTCATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419436_132419441del , CM000667.2:g.132419436_132419441del	GRCh38
NC_000005.9:g.131755128_131755133del , CM000667.1:g.131755128_131755133del	GRCh37
NC_000005.8:g.131783027_131783032del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-387_-326-382del	ENSP00000492349.2:n.-326-387_-326-382del
ENST00000638504.1:n.89-387_89-382del
ENST00000638568.2:c.-468-387_-468-382del	ENSP00000491158.2:n.-468-387_-468-382del
ENST00000639899.1:n.132-387_132-382del
ENST00000337752.6:c.-70-387_-70-382del (CARINH)	ENSP00000338228.2:n.-70-387_-70-382del
ENST00000378947.7:c.-70-387_-70-382del (CARINH)	ENSP00000368230.3:n.-70-387_-70-382del
ENST00000378953.8:c.-70-387_-70-382del (CARINH)	ENSP00000368236.4:n.-70-387_-70-382del
ENST00000407797.5:c.-70-387_-70-382del (CARINH)	ENSP00000385513.1:n.-70-387_-70-382del
ENST00000461203.5:n.62-387_62-382del (CARINH)
NR_045116.1:n.270-387_270-382del (CARINH)
NM_001207001.2:c.-70-387_-70-382del (CARINH)	NP_001193930.1:n.-70-387_-70-382del
XR_948788.3:n.1204_1209del (LINC02863)
NR_161242.1:n.114-387_114-382del (CARINH)