Canonical Allele Identifier: CA446357982

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755593C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419901C>G , CM000667.2:g.132419901C>G	GRCh38
NC_000005.9:g.131755593C>G , CM000667.1:g.131755593C>G	GRCh37
NC_000005.8:g.131783492C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-248C>G	ENSP00000492349.2:n.-248C>G
ENST00000638504.1:n.167C>G
ENST00000638568.2:c.-390C>G	ENSP00000491158.2:n.-390C>G
ENST00000639899.1:n.210C>G
ENST00000337752.6:c.9C>G (CARINH)	ENSP00000338228.2:p.Ser3=
ENST00000378947.7:c.9C>G (CARINH)	ENSP00000368230.3:p.Ser3=
ENST00000378953.8:c.9C>G (CARINH)	ENSP00000368236.4:p.Ser3=
ENST00000407797.5:c.9C>G (CARINH)	ENSP00000385513.1:p.Ser3=
ENST00000461203.5:n.140C>G (CARINH)
ENST00000621237.1:c.9C>G (CARINH)	ENSP00000481774.1:p.Ser3=
NR_045116.1:n.348C>G (CARINH)
NM_001207001.2:c.9C>G (CARINH)	NP_001193930.1:p.Ser3=
XR_948788.3:n.894-152G>C (LINC02863)
NR_161242.1:n.192C>G (CARINH)