Canonical Allele Identifier: CA2822690184

Gene: HNRNPH2 RPL36A-HNRNPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101412793dup , CM000685.2:g.101412793dup	GRCh38
NC_000023.10:g.100667781dup , CM000685.1:g.100667781dup	GRCh37
NC_000023.9:g.100554437dup	NCBI36
NG_007119.1:g.175dup , LRG_672:g.175dup
NG_016327.1:g.9591dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316594.6:c.805dup (HNRNPH2) MANE Select	ENSP00000361927.2:p.Ser269PhefsTer5
ENST00000316594.5:c.805dup (HNRNPH2)	ENSP00000361927.2:p.Ser269PhefsTer5
NM_001032393.2:c.805dup (HNRNPH2)	NP_001027565.1:p.Ser269PhefsTer5
NM_001199973.1:c.*801dup (RPL36A-HNRNPH2)	NP_001186902.1:n.*801dup
NM_001199974.1:c.*801dup (RPL36A-HNRNPH2)	NP_001186903.1:n.*801dup
NM_019597.4:c.805dup (HNRNPH2)	NP_062543.1:p.Ser269PhefsTer5
NM_001199973.2:c.*801dup (RPL36A-HNRNPH2)	NP_001186902.2:n.*801dup
NM_001199974.2:c.*801dup (RPL36A-HNRNPH2)	NP_001186903.2:n.*801dup
NM_019597.5:c.805dup (HNRNPH2) MANE Select	NP_062543.1:p.Ser269PhefsTer5
NM_001032393.3:c.805dup (HNRNPH2)	NP_001027565.1:p.Ser269PhefsTer5