Canonical Allele Identifier: CA2675201573

Gene: CARINH LINC02863

Linked Data

• gnomAD v4: 5-132419837-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419840dup , CM000667.2:g.132419840dup	GRCh38
NC_000005.9:g.131755532dup , CM000667.1:g.131755532dup	GRCh37
NC_000005.8:g.131783431dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-309dup	ENSP00000492349.2:n.-309dup
ENST00000638504.1:n.106dup
ENST00000638568.2:c.-451dup	ENSP00000491158.2:n.-451dup
ENST00000639899.1:n.149dup
ENST00000337752.6:c.-53dup (CARINH)	ENSP00000338228.2:n.-53dup
ENST00000378947.7:c.-53dup (CARINH)	ENSP00000368230.3:n.-53dup
ENST00000378953.8:c.-53dup (CARINH)	ENSP00000368236.4:n.-53dup
ENST00000407797.5:c.-53dup (CARINH)	ENSP00000385513.1:n.-53dup
ENST00000461203.5:n.79dup (CARINH)
NR_045116.1:n.287dup (CARINH)
NM_001207001.2:c.-53dup (CARINH)	NP_001193930.1:n.-53dup
XR_948788.3:n.894-89dup (LINC02863)
NR_161242.1:n.131dup (CARINH)