Canonical Allele Identifier: CA2768436251

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419890A>G , CM000667.2:g.132419890A>G	GRCh38
NC_000005.9:g.131755582A>G , CM000667.1:g.131755582A>G	GRCh37
NC_000005.8:g.131783481A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-259A>G	ENSP00000492349.2:n.-259A>G
ENST00000638504.1:n.156A>G
ENST00000638568.2:c.-401A>G	ENSP00000491158.2:n.-401A>G
ENST00000639899.1:n.199A>G
ENST00000337752.6:c.-3A>G (CARINH)	ENSP00000338228.2:n.-3A>G
ENST00000378947.7:c.-3A>G (CARINH)	ENSP00000368230.3:n.-3A>G
ENST00000378953.8:c.-3A>G (CARINH)	ENSP00000368236.4:n.-3A>G
ENST00000407797.5:c.-3A>G (CARINH)	ENSP00000385513.1:n.-3A>G
ENST00000461203.5:n.129A>G (CARINH)
ENST00000621237.1:c.-3A>G (CARINH)	ENSP00000481774.1:n.-3A>G
NR_045116.1:n.337A>G (CARINH)
NM_001207001.2:c.-3A>G (CARINH)	NP_001193930.1:n.-3A>G
XR_948788.3:n.894-141T>C (LINC02863)
NR_161242.1:n.181A>G (CARINH)