Canonical Allele Identifier: CA446357978

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755590C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419898C>T , CM000667.2:g.132419898C>T	GRCh38
NC_000005.9:g.131755590C>T , CM000667.1:g.131755590C>T	GRCh37
NC_000005.8:g.131783489C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-251C>T	ENSP00000492349.2:n.-251C>T
ENST00000638504.1:n.164C>T
ENST00000638568.2:c.-393C>T	ENSP00000491158.2:n.-393C>T
ENST00000639899.1:n.207C>T
ENST00000337752.6:c.6C>T (CARINH)	ENSP00000338228.2:p.Asp2=
ENST00000378947.7:c.6C>T (CARINH)	ENSP00000368230.3:p.Asp2=
ENST00000378953.8:c.6C>T (CARINH)	ENSP00000368236.4:p.Asp2=
ENST00000407797.5:c.6C>T (CARINH)	ENSP00000385513.1:p.Asp2=
ENST00000461203.5:n.137C>T (CARINH)
ENST00000621237.1:c.6C>T (CARINH)	ENSP00000481774.1:p.Asp2=
NR_045116.1:n.345C>T (CARINH)
NM_001207001.2:c.6C>T (CARINH)	NP_001193930.1:p.Asp2=
XR_948788.3:n.894-149G>A (LINC02863)
NR_161242.1:n.189C>T (CARINH)