Canonical Allele Identifier: CA360812418

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755618A>G (hg19) ; chr5:g.132419926A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419926A>G , CM000667.2:g.132419926A>G	GRCh38
NC_000005.9:g.131755618A>G , CM000667.1:g.131755618A>G	GRCh37
NC_000005.8:g.131783517A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-223A>G	ENSP00000492349.2:n.-223A>G
ENST00000638504.1:n.192A>G
ENST00000638568.2:c.-365A>G	ENSP00000491158.2:n.-365A>G
ENST00000639899.1:n.235A>G
ENST00000337752.6:c.34A>G (CARINH)	ENSP00000338228.2:p.Ser12Gly
ENST00000378947.7:c.34A>G (CARINH)	ENSP00000368230.3:p.Ser12Gly
ENST00000378953.8:c.34A>G (CARINH)	ENSP00000368236.4:p.Ser12Gly
ENST00000407797.5:c.34A>G (CARINH)	ENSP00000385513.1:p.Ser12Gly
ENST00000461203.5:n.165A>G (CARINH)
ENST00000621237.1:c.34A>G (CARINH)	ENSP00000481774.1:p.Ser12Gly
NR_045116.1:n.373A>G (CARINH)
NM_001207001.2:c.34A>G (CARINH)	NP_001193930.1:p.Ser12Gly
XR_948788.3:n.894-177T>C (LINC02863)
NR_161242.1:n.217A>G (CARINH)