Canonical Allele Identifier: CA517737597

Gene: HNRNPH2 RPL36A-HNRNPH2

Linked Data

• COSMIC: COSM1464413
• MyVariant Identifiers: chrX:g.100667857del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101412873del , CM000685.2:g.101412873del	GRCh38
NC_000023.10:g.100667861del , CM000685.1:g.100667861del	GRCh37
NC_000023.9:g.100554517del	NCBI36
NG_007119.1:g.95del , LRG_672:g.95del
NG_016327.1:g.9671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316594.6:c.885del (HNRNPH2) MANE Select	ENSP00000361927.2:p.Leu296TyrfsTer20
ENST00000316594.5:c.885del (HNRNPH2)	ENSP00000361927.2:p.Leu296TyrfsTer20
NM_001032393.2:c.885del (HNRNPH2)	NP_001027565.1:p.Leu296TyrfsTer20
NM_001199973.1:c.*881del (RPL36A-HNRNPH2)	NP_001186902.1:n.*881del
NM_001199974.1:c.*881del (RPL36A-HNRNPH2)	NP_001186903.1:n.*881del
NM_019597.4:c.885del (HNRNPH2)	NP_062543.1:p.Leu296TyrfsTer20
NM_001199973.2:c.*881del (RPL36A-HNRNPH2)	NP_001186902.2:n.*881del
NM_001199974.2:c.*881del (RPL36A-HNRNPH2)	NP_001186903.2:n.*881del
NM_019597.5:c.885del (HNRNPH2) MANE Select	NP_062543.1:p.Leu296TyrfsTer20
NM_001032393.3:c.885del (HNRNPH2)	NP_001027565.1:p.Leu296TyrfsTer20