Canonical Allele Identifier: CA2579664664
Gene: HNRNPH2 HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101412710_101412718del , CM000685.2:g.101412710_101412718del GRCh38
NC_000023.10:g.100667698_100667706del , CM000685.1:g.100667698_100667706del GRCh37
NC_000023.9:g.100554354_100554362del NCBI36
NG_007119.1:g.250_258del , LRG_672:g.250_258del
NG_016327.1:g.9508_9516del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316594.6:c.722_730del (HNRNPH2) MANE Select ENSP00000361927.2:p.Gly241_Tyr243del
ENST00000316594.5:c.722_730del (HNRNPH2) ENSP00000361927.2:p.Gly241_Tyr243del
NM_001032393.2:c.722_730del (HNRNPH2) NP_001027565.1:p.Gly241_Tyr243del
NM_001199973.1:c.*718_*726del (RPL36A-HNRNPH2) NP_001186902.1:n.*718_*726del
NM_001199974.1:c.*718_*726del (RPL36A-HNRNPH2) NP_001186903.1:n.*718_*726del
NM_019597.4:c.722_730del (HNRNPH2) NP_062543.1:p.Gly241_Tyr243del
NM_001199973.2:c.*718_*726del (RPL36A-HNRNPH2) NP_001186902.2:n.*718_*726del
NM_001199974.2:c.*718_*726del (RPL36A-HNRNPH2) NP_001186903.2:n.*718_*726del
NM_019597.5:c.722_730del (HNRNPH2) MANE Select NP_062543.1:p.Gly241_Tyr243del
NM_001032393.3:c.722_730del (HNRNPH2) NP_001027565.1:p.Gly241_Tyr243del