Canonical Allele Identifier: CA2675201613

Gene: CARINH LINC02863

Linked Data

• gnomAD v4: 5-132419877-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419878dup , CM000667.2:g.132419878dup	GRCh38
NC_000005.9:g.131755570dup , CM000667.1:g.131755570dup	GRCh37
NC_000005.8:g.131783469dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-271dup	ENSP00000492349.2:n.-271dup
ENST00000638504.1:n.144dup
ENST00000638568.2:c.-413dup	ENSP00000491158.2:n.-413dup
ENST00000639899.1:n.187dup
ENST00000337752.6:c.-15dup (CARINH)	ENSP00000338228.2:n.-15dup
ENST00000378947.7:c.-15dup (CARINH)	ENSP00000368230.3:n.-15dup
ENST00000378953.8:c.-15dup (CARINH)	ENSP00000368236.4:n.-15dup
ENST00000407797.5:c.-15dup (CARINH)	ENSP00000385513.1:n.-15dup
ENST00000461203.5:n.117dup (CARINH)
ENST00000621237.1:c.-15dup (CARINH)	ENSP00000481774.1:n.-15dup
NR_045116.1:n.325dup (CARINH)
NM_001207001.2:c.-15dup (CARINH)	NP_001193930.1:n.-15dup
XR_948788.3:n.894-129dup (LINC02863)
NR_161242.1:n.169dup (CARINH)