Canonical Allele Identifier: CA650289635

Gene: CARINH LINC02863

Linked Data

• COSMIC: COSN22814366

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132420018del , CM000667.2:g.132420018del	GRCh38
NC_000005.9:g.131755710del , CM000667.1:g.131755710del	GRCh37
NC_000005.8:g.131783609del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-209+78del	ENSP00000492349.2:n.-209+78del
ENST00000638504.1:n.206+78del
ENST00000638568.2:c.-351+78del	ENSP00000491158.2:n.-351+78del
ENST00000639899.1:n.249+78del
ENST00000337752.6:c.48+78del (CARINH)	ENSP00000338228.2:n.48+78del
ENST00000378947.7:c.48+78del (CARINH)	ENSP00000368230.3:n.48+78del
ENST00000378953.8:c.48+78del (CARINH)	ENSP00000368236.4:n.48+78del
ENST00000407797.5:c.48+78del (CARINH)	ENSP00000385513.1:n.48+78del
ENST00000461203.5:n.179+78del (CARINH)
ENST00000621237.1:c.48+78del (CARINH)	ENSP00000481774.1:n.48+78del
NR_045116.1:n.387+78del (CARINH)
NM_001207001.2:c.48+78del (CARINH)	NP_001193930.1:n.48+78del
XR_948788.3:n.894-267del (LINC02863)
NR_161242.1:n.231+78del (CARINH)