Canonical Allele Identifier: CA127223479

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs917767331
• gnomAD v2: 5-131755100-CTT-C
• gnomAD v3: 5-132419408-CTT-C
• gnomAD v4: 5-132419408-CTT-C
• MyVariant Identifiers: chr5:g.131755101_131755102del (hg19) ; chr5:g.132419409_132419410del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419410_132419411del , CM000667.2:g.132419410_132419411del	GRCh38
NC_000005.9:g.131755102_131755103del , CM000667.1:g.131755102_131755103del	GRCh37
NC_000005.8:g.131783001_131783002del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-413_-326-412del	ENSP00000492349.2:n.-326-413_-326-412del
ENST00000638504.1:n.89-413_89-412del
ENST00000638568.2:c.-468-413_-468-412del	ENSP00000491158.2:n.-468-413_-468-412del
ENST00000639899.1:n.132-413_132-412del
ENST00000337752.6:c.-70-413_-70-412del (CARINH)	ENSP00000338228.2:n.-70-413_-70-412del
ENST00000378947.7:c.-70-413_-70-412del (CARINH)	ENSP00000368230.3:n.-70-413_-70-412del
ENST00000378953.8:c.-70-413_-70-412del (CARINH)	ENSP00000368236.4:n.-70-413_-70-412del
ENST00000407797.5:c.-70-413_-70-412del (CARINH)	ENSP00000385513.1:n.-70-413_-70-412del
ENST00000461203.5:n.62-413_62-412del (CARINH)
NR_045116.1:n.270-413_270-412del (CARINH)
NM_001207001.2:c.-70-413_-70-412del (CARINH)	NP_001193930.1:n.-70-413_-70-412del
XR_948788.3:n.1233_1234del (LINC02863)
NR_161242.1:n.114-413_114-412del (CARINH)