Canonical Allele Identifier: CA360812506

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755630T>G (hg19) ; chr5:g.132419938T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419938T>G , CM000667.2:g.132419938T>G	GRCh38
NC_000005.9:g.131755630T>G , CM000667.1:g.131755630T>G	GRCh37
NC_000005.8:g.131783529T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-211T>G	ENSP00000492349.2:n.-211T>G
ENST00000638504.1:n.204T>G
ENST00000638568.2:c.-353T>G	ENSP00000491158.2:n.-353T>G
ENST00000639899.1:n.247T>G
ENST00000337752.6:c.46T>G (CARINH)	ENSP00000338228.2:p.Trp16Gly
ENST00000378947.7:c.46T>G (CARINH)	ENSP00000368230.3:p.Trp16Gly
ENST00000378953.8:c.46T>G (CARINH)	ENSP00000368236.4:p.Trp16Gly
ENST00000407797.5:c.46T>G (CARINH)	ENSP00000385513.1:p.Trp16Gly
ENST00000461203.5:n.177T>G (CARINH)
ENST00000621237.1:c.46T>G (CARINH)	ENSP00000481774.1:p.Trp16Gly
NR_045116.1:n.385T>G (CARINH)
NM_001207001.2:c.46T>G (CARINH)	NP_001193930.1:p.Trp16Gly
XR_948788.3:n.894-189A>C (LINC02863)
NR_161242.1:n.229T>G (CARINH)