Canonical Allele Identifier: CA1081638141

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1753232777
• gnomAD v3: 5-132419794-CTTATGTTTTTTCCTTGT-C
• gnomAD v4: 5-132419794-CTTATGTTTTTTCCTTGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419797_132419813del , CM000667.2:g.132419797_132419813del	GRCh38
NC_000005.9:g.131755489_131755505del , CM000667.1:g.131755489_131755505del	GRCh37
NC_000005.8:g.131783388_131783404del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-26_-326-10del	ENSP00000492349.2:n.-326-26_-326-10del
ENST00000638504.1:n.89-26_89-10del
ENST00000638568.2:c.-468-26_-468-10del	ENSP00000491158.2:n.-468-26_-468-10del
ENST00000639899.1:n.132-26_132-10del
ENST00000337752.6:c.-70-26_-70-10del (CARINH)	ENSP00000338228.2:n.-70-26_-70-10del
ENST00000378947.7:c.-70-26_-70-10del (CARINH)	ENSP00000368230.3:n.-70-26_-70-10del
ENST00000378953.8:c.-70-26_-70-10del (CARINH)	ENSP00000368236.4:n.-70-26_-70-10del
ENST00000407797.5:c.-70-26_-70-10del (CARINH)	ENSP00000385513.1:n.-70-26_-70-10del
ENST00000461203.5:n.62-26_62-10del (CARINH)
NR_045116.1:n.270-26_270-10del (CARINH)
NM_001207001.2:c.-70-26_-70-10del (CARINH)	NP_001193930.1:n.-70-26_-70-10del
XR_948788.3:n.894-62_894-46del (LINC02863)
NR_161242.1:n.114-26_114-10del (CARINH)