Canonical Allele Identifier: CA360812338

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755608G>C (hg19) ; chr5:g.132419916G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419916G>C , CM000667.2:g.132419916G>C	GRCh38
NC_000005.9:g.131755608G>C , CM000667.1:g.131755608G>C	GRCh37
NC_000005.8:g.131783507G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-233G>C	ENSP00000492349.2:n.-233G>C
ENST00000638504.1:n.182G>C
ENST00000638568.2:c.-375G>C	ENSP00000491158.2:n.-375G>C
ENST00000639899.1:n.225G>C
ENST00000337752.6:c.24G>C (CARINH)	ENSP00000338228.2:p.Glu8Asp
ENST00000378947.7:c.24G>C (CARINH)	ENSP00000368230.3:p.Glu8Asp
ENST00000378953.8:c.24G>C (CARINH)	ENSP00000368236.4:p.Glu8Asp
ENST00000407797.5:c.24G>C (CARINH)	ENSP00000385513.1:p.Glu8Asp
ENST00000461203.5:n.155G>C (CARINH)
ENST00000621237.1:c.24G>C (CARINH)	ENSP00000481774.1:p.Glu8Asp
NR_045116.1:n.363G>C (CARINH)
NM_001207001.2:c.24G>C (CARINH)	NP_001193930.1:p.Glu8Asp
XR_948788.3:n.894-167C>G (LINC02863)
NR_161242.1:n.207G>C (CARINH)