Canonical Allele Identifier: CA3015135183

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419873G>C , CM000667.2:g.132419873G>C	GRCh38
NC_000005.9:g.131755565G>C , CM000667.1:g.131755565G>C	GRCh37
NC_000005.8:g.131783464G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-276G>C	ENSP00000492349.2:n.-276G>C
ENST00000638504.1:n.139G>C
ENST00000638568.2:c.-418G>C	ENSP00000491158.2:n.-418G>C
ENST00000639899.1:n.182G>C
ENST00000337752.6:c.-20G>C (CARINH)	ENSP00000338228.2:n.-20G>C
ENST00000378947.7:c.-20G>C (CARINH)	ENSP00000368230.3:n.-20G>C
ENST00000378953.8:c.-20G>C (CARINH)	ENSP00000368236.4:n.-20G>C
ENST00000407797.5:c.-20G>C (CARINH)	ENSP00000385513.1:n.-20G>C
ENST00000461203.5:n.112G>C (CARINH)
ENST00000621237.1:c.-20G>C (CARINH)	ENSP00000481774.1:n.-20G>C
NR_045116.1:n.320G>C (CARINH)
NM_001207001.2:c.-20G>C (CARINH)	NP_001193930.1:n.-20G>C
XR_948788.3:n.894-124C>G (LINC02863)
NR_161242.1:n.164G>C (CARINH)