Canonical Allele Identifier: CA360812253

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755591T>A (hg19) ; chr5:g.132419899T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419899T>A , CM000667.2:g.132419899T>A	GRCh38
NC_000005.9:g.131755591T>A , CM000667.1:g.131755591T>A	GRCh37
NC_000005.8:g.131783490T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-250T>A	ENSP00000492349.2:n.-250T>A
ENST00000638504.1:n.165T>A
ENST00000638568.2:c.-392T>A	ENSP00000491158.2:n.-392T>A
ENST00000639899.1:n.208T>A
ENST00000337752.6:c.7T>A (CARINH)	ENSP00000338228.2:p.Ser3Thr
ENST00000378947.7:c.7T>A (CARINH)	ENSP00000368230.3:p.Ser3Thr
ENST00000378953.8:c.7T>A (CARINH)	ENSP00000368236.4:p.Ser3Thr
ENST00000407797.5:c.7T>A (CARINH)	ENSP00000385513.1:p.Ser3Thr
ENST00000461203.5:n.138T>A (CARINH)
ENST00000621237.1:c.7T>A (CARINH)	ENSP00000481774.1:p.Ser3Thr
NR_045116.1:n.346T>A (CARINH)
NM_001207001.2:c.7T>A (CARINH)	NP_001193930.1:p.Ser3Thr
XR_948788.3:n.894-150A>T (LINC02863)
NR_161242.1:n.190T>A (CARINH)