Canonical Allele Identifier: CA2984463972

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419876A>T , CM000667.2:g.132419876A>T	GRCh38
NC_000005.9:g.131755568A>T , CM000667.1:g.131755568A>T	GRCh37
NC_000005.8:g.131783467A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-273A>T	ENSP00000492349.2:n.-273A>T
ENST00000638504.1:n.142A>T
ENST00000638568.2:c.-415A>T	ENSP00000491158.2:n.-415A>T
ENST00000639899.1:n.185A>T
ENST00000337752.6:c.-17A>T (CARINH)	ENSP00000338228.2:n.-17A>T
ENST00000378947.7:c.-17A>T (CARINH)	ENSP00000368230.3:n.-17A>T
ENST00000378953.8:c.-17A>T (CARINH)	ENSP00000368236.4:n.-17A>T
ENST00000407797.5:c.-17A>T (CARINH)	ENSP00000385513.1:n.-17A>T
ENST00000461203.5:n.115A>T (CARINH)
ENST00000621237.1:c.-17A>T (CARINH)	ENSP00000481774.1:n.-17A>T
NR_045116.1:n.323A>T (CARINH)
NM_001207001.2:c.-17A>T (CARINH)	NP_001193930.1:n.-17A>T
XR_948788.3:n.894-127T>A (LINC02863)
NR_161242.1:n.167A>T (CARINH)