Canonical Allele Identifier: CA3404256

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs775510403
• ExAC: 5:131755624 C / A
• gnomAD v2: 5-131755624-C-A
• gnomAD v4: 5-132419932-C-A
• MyVariant Identifiers: chr5:g.131755624C>A (hg19) ; chr5:g.132419932C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419932C>A , CM000667.2:g.132419932C>A	GRCh38
NC_000005.9:g.131755624C>A , CM000667.1:g.131755624C>A	GRCh37
NC_000005.8:g.131783523C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-217C>A	ENSP00000492349.2:n.-217C>A
ENST00000638504.1:n.198C>A
ENST00000638568.2:c.-359C>A	ENSP00000491158.2:n.-359C>A
ENST00000639899.1:n.241C>A
ENST00000337752.6:c.40C>A (CARINH)	ENSP00000338228.2:p.Gln14Lys
ENST00000378947.7:c.40C>A (CARINH)	ENSP00000368230.3:p.Gln14Lys
ENST00000378953.8:c.40C>A (CARINH)	ENSP00000368236.4:p.Gln14Lys
ENST00000407797.5:c.40C>A (CARINH)	ENSP00000385513.1:p.Gln14Lys
ENST00000461203.5:n.171C>A (CARINH)
ENST00000621237.1:c.40C>A (CARINH)	ENSP00000481774.1:p.Gln14Lys
NR_045116.1:n.379C>A (CARINH)
NM_001207001.2:c.40C>A (CARINH)	NP_001193930.1:p.Gln14Lys
XR_948788.3:n.894-183G>T (LINC02863)
NR_161242.1:n.223C>A (CARINH)