Canonical Allele Identifier: CA446358002

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755605A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419913A>C , CM000667.2:g.132419913A>C	GRCh38
NC_000005.9:g.131755605A>C , CM000667.1:g.131755605A>C	GRCh37
NC_000005.8:g.131783504A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-236A>C	ENSP00000492349.2:n.-236A>C
ENST00000638504.1:n.179A>C
ENST00000638568.2:c.-378A>C	ENSP00000491158.2:n.-378A>C
ENST00000639899.1:n.222A>C
ENST00000337752.6:c.21A>C (CARINH)	ENSP00000338228.2:p.Gly7=
ENST00000378947.7:c.21A>C (CARINH)	ENSP00000368230.3:p.Gly7=
ENST00000378953.8:c.21A>C (CARINH)	ENSP00000368236.4:p.Gly7=
ENST00000407797.5:c.21A>C (CARINH)	ENSP00000385513.1:p.Gly7=
ENST00000461203.5:n.152A>C (CARINH)
ENST00000621237.1:c.21A>C (CARINH)	ENSP00000481774.1:p.Gly7=
NR_045116.1:n.360A>C (CARINH)
NM_001207001.2:c.21A>C (CARINH)	NP_001193930.1:p.Gly7=
XR_948788.3:n.894-164T>G (LINC02863)
NR_161242.1:n.204A>C (CARINH)