Canonical Allele Identifier: CA2984463968

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419870A>T , CM000667.2:g.132419870A>T	GRCh38
NC_000005.9:g.131755562A>T , CM000667.1:g.131755562A>T	GRCh37
NC_000005.8:g.131783461A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-279A>T	ENSP00000492349.2:n.-279A>T
ENST00000638504.1:n.136A>T
ENST00000638568.2:c.-421A>T	ENSP00000491158.2:n.-421A>T
ENST00000639899.1:n.179A>T
ENST00000337752.6:c.-23A>T (CARINH)	ENSP00000338228.2:n.-23A>T
ENST00000378947.7:c.-23A>T (CARINH)	ENSP00000368230.3:n.-23A>T
ENST00000378953.8:c.-23A>T (CARINH)	ENSP00000368236.4:n.-23A>T
ENST00000407797.5:c.-23A>T (CARINH)	ENSP00000385513.1:n.-23A>T
ENST00000461203.5:n.109A>T (CARINH)
ENST00000621237.1:c.-23A>T (CARINH)	ENSP00000481774.1:n.-23A>T
NR_045116.1:n.317A>T (CARINH)
NM_001207001.2:c.-23A>T (CARINH)	NP_001193930.1:n.-23A>T
XR_948788.3:n.894-121T>A (LINC02863)
NR_161242.1:n.161A>T (CARINH)