Canonical Allele Identifier: CA2768436257

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419967T>A , CM000667.2:g.132419967T>A	GRCh38
NC_000005.9:g.131755659T>A , CM000667.1:g.131755659T>A	GRCh37
NC_000005.8:g.131783558T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-209+27T>A	ENSP00000492349.2:n.-209+27T>A
ENST00000638504.1:n.206+27T>A
ENST00000638568.2:c.-351+27T>A	ENSP00000491158.2:n.-351+27T>A
ENST00000639899.1:n.249+27T>A
ENST00000337752.6:c.48+27T>A (CARINH)	ENSP00000338228.2:n.48+27T>A
ENST00000378947.7:c.48+27T>A (CARINH)	ENSP00000368230.3:n.48+27T>A
ENST00000378953.8:c.48+27T>A (CARINH)	ENSP00000368236.4:n.48+27T>A
ENST00000407797.5:c.48+27T>A (CARINH)	ENSP00000385513.1:n.48+27T>A
ENST00000461203.5:n.179+27T>A (CARINH)
ENST00000621237.1:c.48+27T>A (CARINH)	ENSP00000481774.1:n.48+27T>A
NR_045116.1:n.387+27T>A (CARINH)
NM_001207001.2:c.48+27T>A (CARINH)	NP_001193930.1:n.48+27T>A
XR_948788.3:n.894-218A>T (LINC02863)
NR_161242.1:n.231+27T>A (CARINH)