Canonical Allele Identifier: CA360812368

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755613A>C (hg19) ; chr5:g.132419921A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419921A>C , CM000667.2:g.132419921A>C	GRCh38
NC_000005.9:g.131755613A>C , CM000667.1:g.131755613A>C	GRCh37
NC_000005.8:g.131783512A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-228A>C	ENSP00000492349.2:n.-228A>C
ENST00000638504.1:n.187A>C
ENST00000638568.2:c.-370A>C	ENSP00000491158.2:n.-370A>C
ENST00000639899.1:n.230A>C
ENST00000337752.6:c.29A>C (CARINH)	ENSP00000338228.2:p.Asn10Thr
ENST00000378947.7:c.29A>C (CARINH)	ENSP00000368230.3:p.Asn10Thr
ENST00000378953.8:c.29A>C (CARINH)	ENSP00000368236.4:p.Asn10Thr
ENST00000407797.5:c.29A>C (CARINH)	ENSP00000385513.1:p.Asn10Thr
ENST00000461203.5:n.160A>C (CARINH)
ENST00000621237.1:c.29A>C (CARINH)	ENSP00000481774.1:p.Asn10Thr
NR_045116.1:n.368A>C (CARINH)
NM_001207001.2:c.29A>C (CARINH)	NP_001193930.1:p.Asn10Thr
XR_948788.3:n.894-172T>G (LINC02863)
NR_161242.1:n.212A>C (CARINH)