Canonical Allele Identifier: CA803996217

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1413575468
• gnomAD v3: 5-132419619-T-TA
• gnomAD v4: 5-132419619-T-TA
• MyVariant Identifiers: chr5:g.131755311_131755312insA (hg19) ; chr5:g.132419619_132419620insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419620dup , CM000667.2:g.132419620dup	GRCh38
NC_000005.9:g.131755312dup , CM000667.1:g.131755312dup	GRCh37
NC_000005.8:g.131783211dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-203dup	ENSP00000492349.2:n.-326-203dup
ENST00000638504.1:n.89-203dup
ENST00000638568.2:c.-468-203dup	ENSP00000491158.2:n.-468-203dup
ENST00000639899.1:n.132-203dup
ENST00000337752.6:c.-70-203dup (CARINH)	ENSP00000338228.2:n.-70-203dup
ENST00000378947.7:c.-70-203dup (CARINH)	ENSP00000368230.3:n.-70-203dup
ENST00000378953.8:c.-70-203dup (CARINH)	ENSP00000368236.4:n.-70-203dup
ENST00000407797.5:c.-70-203dup (CARINH)	ENSP00000385513.1:n.-70-203dup
ENST00000461203.5:n.62-203dup (CARINH)
NR_045116.1:n.270-203dup (CARINH)
NM_001207001.2:c.-70-203dup (CARINH)	NP_001193930.1:n.-70-203dup
XR_948788.3:n.1023dup (LINC02863)
NR_161242.1:n.114-203dup (CARINH)