Canonical Allele Identifier: CA2984463989

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419971_132419972del , CM000667.2:g.132419971_132419972del	GRCh38
NC_000005.9:g.131755663_131755664del , CM000667.1:g.131755663_131755664del	GRCh37
NC_000005.8:g.131783562_131783563del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-209+31_-209+32del	ENSP00000492349.2:n.-209+31_-209+32del
ENST00000638504.1:n.206+31_206+32del
ENST00000638568.2:c.-351+31_-351+32del	ENSP00000491158.2:n.-351+31_-351+32del
ENST00000639899.1:n.249+31_249+32del
ENST00000337752.6:c.48+31_48+32del (CARINH)	ENSP00000338228.2:n.48+31_48+32del
ENST00000378947.7:c.48+31_48+32del (CARINH)	ENSP00000368230.3:n.48+31_48+32del
ENST00000378953.8:c.48+31_48+32del (CARINH)	ENSP00000368236.4:n.48+31_48+32del
ENST00000407797.5:c.48+31_48+32del (CARINH)	ENSP00000385513.1:n.48+31_48+32del
ENST00000461203.5:n.179+31_179+32del (CARINH)
ENST00000621237.1:c.48+31_48+32del (CARINH)	ENSP00000481774.1:n.48+31_48+32del
NR_045116.1:n.387+31_387+32del (CARINH)
NM_001207001.2:c.48+31_48+32del (CARINH)	NP_001193930.1:n.48+31_48+32del
XR_948788.3:n.894-220_894-219del (LINC02863)
NR_161242.1:n.231+31_231+32del (CARINH)