Canonical Allele Identifier: CA1583158774

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132420276_132420277delinsTC , CM000667.2:g.132420276_132420277delinsTC	GRCh38
NC_000005.9:g.131755968_131755969delinsTC , CM000667.1:g.131755968_131755969delinsTC	GRCh37
NC_000005.8:g.131783867_131783868delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-209+336_-209+337delinsTC	ENSP00000492349.2:n.-209+336_-209+337delinsTC
ENST00000638504.1:n.206+336_206+337delinsTC
ENST00000638568.2:c.-351+336_-351+337delinsTC	ENSP00000491158.2:n.-351+336_-351+337delinsTC
ENST00000639899.1:n.249+336_249+337delinsTC
ENST00000337752.6:c.48+336_48+337delinsTC (CARINH)	ENSP00000338228.2:n.48+336_48+337delinsTC
ENST00000378947.7:c.48+336_48+337delinsTC (CARINH)	ENSP00000368230.3:n.48+336_48+337delinsTC
ENST00000378953.8:c.48+336_48+337delinsTC (CARINH)	ENSP00000368236.4:n.48+336_48+337delinsTC
ENST00000407797.5:c.48+336_48+337delinsTC (CARINH)	ENSP00000385513.1:n.48+336_48+337delinsTC
ENST00000461203.5:n.179+336_179+337delinsTC (CARINH)
ENST00000621237.1:c.48+336_48+337delinsTC (CARINH)	ENSP00000481774.1:n.48+336_48+337delinsTC
NR_045116.1:n.387+336_387+337delinsTC (CARINH)
NM_001207001.2:c.48+336_48+337delinsTC (CARINH)	NP_001193930.1:n.48+336_48+337delinsTC
XR_948788.3:n.894-528_894-527delinsGA (LINC02863)
NR_161242.1:n.231+336_231+337delinsTC (CARINH)