Canonical Allele Identifier: CA2822690182

Gene: HNRNPH2 RPL36A-HNRNPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101412497_101412498insAC , CM000685.2:g.101412497_101412498insAC	GRCh38
NC_000023.10:g.100667485_100667486insAC , CM000685.1:g.100667485_100667486insAC	GRCh37
NC_000023.9:g.100554141_100554142insAC	NCBI36
NG_007119.1:g.466_467insGT , LRG_672:g.466_467insGT
NG_016327.1:g.9295_9296insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316594.6:c.509_510insAC (HNRNPH2) MANE Select	ENSP00000361927.2:p.Lys171ArgfsTer7
ENST00000316594.5:c.509_510insAC (HNRNPH2)	ENSP00000361927.2:p.Lys171ArgfsTer7
NM_001032393.2:c.509_510insAC (HNRNPH2)	NP_001027565.1:p.Lys171ArgfsTer7
NM_001199973.1:c.*505_*506insAC (RPL36A-HNRNPH2)	NP_001186902.1:n.*505_*506insAC
NM_001199974.1:c.*505_*506insAC (RPL36A-HNRNPH2)	NP_001186903.1:n.*505_*506insAC
NM_019597.4:c.509_510insAC (HNRNPH2)	NP_062543.1:p.Lys171ArgfsTer7
NM_001199973.2:c.*505_*506insAC (RPL36A-HNRNPH2)	NP_001186902.2:n.*505_*506insAC
NM_001199974.2:c.*505_*506insAC (RPL36A-HNRNPH2)	NP_001186903.2:n.*505_*506insAC
NM_019597.5:c.509_510insAC (HNRNPH2) MANE Select	NP_062543.1:p.Lys171ArgfsTer7
NM_001032393.3:c.509_510insAC (HNRNPH2)	NP_001027565.1:p.Lys171ArgfsTer7