Canonical Allele Identifier: CA127223523

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs555823527
• gnomAD v2: 5-131755164-AAT-A
• gnomAD v3: 5-132419472-AAT-A
• gnomAD v4: 5-132419472-AAT-A
• MyVariant Identifiers: chr5:g.131755165_131755166del (hg19) ; chr5:g.132419473_132419474del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419473_132419474del , CM000667.2:g.132419473_132419474del	GRCh38
NC_000005.9:g.131755165_131755166del , CM000667.1:g.131755165_131755166del	GRCh37
NC_000005.8:g.131783064_131783065del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-350_-326-349del	ENSP00000492349.2:n.-326-350_-326-349del
ENST00000638504.1:n.89-350_89-349del
ENST00000638568.2:c.-468-350_-468-349del	ENSP00000491158.2:n.-468-350_-468-349del
ENST00000639899.1:n.132-350_132-349del
ENST00000337752.6:c.-70-350_-70-349del (CARINH)	ENSP00000338228.2:n.-70-350_-70-349del
ENST00000378947.7:c.-70-350_-70-349del (CARINH)	ENSP00000368230.3:n.-70-350_-70-349del
ENST00000378953.8:c.-70-350_-70-349del (CARINH)	ENSP00000368236.4:n.-70-350_-70-349del
ENST00000407797.5:c.-70-350_-70-349del (CARINH)	ENSP00000385513.1:n.-70-350_-70-349del
ENST00000461203.5:n.62-350_62-349del (CARINH)
NR_045116.1:n.270-350_270-349del (CARINH)
NM_001207001.2:c.-70-350_-70-349del (CARINH)	NP_001193930.1:n.-70-350_-70-349del
XR_948788.3:n.1169_1170del (LINC02863)
NR_161242.1:n.114-350_114-349del (CARINH)