Canonical Allele Identifier: CA2768436249

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419866G>A , CM000667.2:g.132419866G>A	GRCh38
NC_000005.9:g.131755558G>A , CM000667.1:g.131755558G>A	GRCh37
NC_000005.8:g.131783457G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-283G>A	ENSP00000492349.2:n.-283G>A
ENST00000638504.1:n.132G>A
ENST00000638568.2:c.-425G>A	ENSP00000491158.2:n.-425G>A
ENST00000639899.1:n.175G>A
ENST00000337752.6:c.-27G>A (CARINH)	ENSP00000338228.2:n.-27G>A
ENST00000378947.7:c.-27G>A (CARINH)	ENSP00000368230.3:n.-27G>A
ENST00000378953.8:c.-27G>A (CARINH)	ENSP00000368236.4:n.-27G>A
ENST00000407797.5:c.-27G>A (CARINH)	ENSP00000385513.1:n.-27G>A
ENST00000461203.5:n.105G>A (CARINH)
ENST00000621237.1:c.-27G>A (CARINH)	ENSP00000481774.1:n.-27G>A
NR_045116.1:n.313G>A (CARINH)
NM_001207001.2:c.-27G>A (CARINH)	NP_001193930.1:n.-27G>A
XR_948788.3:n.894-117C>T (LINC02863)
NR_161242.1:n.157G>A (CARINH)