Canonical Allele Identifier: CA1583158815

Gene: CARINH LINC02863

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132420360_132420361delinsGT , CM000667.2:g.132420360_132420361delinsGT	GRCh38
NC_000005.9:g.131756052_131756053delinsGT , CM000667.1:g.131756052_131756053delinsGT	GRCh37
NC_000005.8:g.131783951_131783952delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-209+420_-209+421delinsGT	ENSP00000492349.2:n.-209+420_-209+421delinsGT
ENST00000638504.1:n.206+420_206+421delinsGT
ENST00000638568.2:c.-351+420_-351+421delinsGT	ENSP00000491158.2:n.-351+420_-351+421delinsGT
ENST00000639899.1:n.249+420_249+421delinsGT
ENST00000337752.6:c.48+420_48+421delinsGT (CARINH)	ENSP00000338228.2:n.48+420_48+421delinsGT
ENST00000378947.7:c.48+420_48+421delinsGT (CARINH)	ENSP00000368230.3:n.48+420_48+421delinsGT
ENST00000378953.8:c.48+420_48+421delinsGT (CARINH)	ENSP00000368236.4:n.48+420_48+421delinsGT
ENST00000407797.5:c.48+420_48+421delinsGT (CARINH)	ENSP00000385513.1:n.48+420_48+421delinsGT
ENST00000461203.5:n.179+420_179+421delinsGT (CARINH)
ENST00000621237.1:c.48+420_48+421delinsGT (CARINH)	ENSP00000481774.1:n.48+420_48+421delinsGT
NR_045116.1:n.387+420_387+421delinsGT (CARINH)
NM_001207001.2:c.48+420_48+421delinsGT (CARINH)	NP_001193930.1:n.48+420_48+421delinsGT
XR_948788.3:n.894-612_894-611delinsAC (LINC02863)
NR_161242.1:n.231+420_231+421delinsGT (CARINH)