Canonical Allele Identifier: CA360812321

Gene: CARINH LINC02863

Linked Data

• COSMIC: COSM357620
• MyVariant Identifiers: chr5:g.131755606G>A (hg19) ; chr5:g.132419914G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419914G>A , CM000667.2:g.132419914G>A	GRCh38
NC_000005.9:g.131755606G>A , CM000667.1:g.131755606G>A	GRCh37
NC_000005.8:g.131783505G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-235G>A	ENSP00000492349.2:n.-235G>A
ENST00000638504.1:n.180G>A
ENST00000638568.2:c.-377G>A	ENSP00000491158.2:n.-377G>A
ENST00000639899.1:n.223G>A
ENST00000337752.6:c.22G>A (CARINH)	ENSP00000338228.2:p.Glu8Lys
ENST00000378947.7:c.22G>A (CARINH)	ENSP00000368230.3:p.Glu8Lys
ENST00000378953.8:c.22G>A (CARINH)	ENSP00000368236.4:p.Glu8Lys
ENST00000407797.5:c.22G>A (CARINH)	ENSP00000385513.1:p.Glu8Lys
ENST00000461203.5:n.153G>A (CARINH)
ENST00000621237.1:c.22G>A (CARINH)	ENSP00000481774.1:p.Glu8Lys
NR_045116.1:n.361G>A (CARINH)
NM_001207001.2:c.22G>A (CARINH)	NP_001193930.1:p.Glu8Lys
XR_948788.3:n.894-165C>T (LINC02863)
NR_161242.1:n.205G>A (CARINH)