Canonical Allele Identifier: CA2448303070

Gene: HNRNPH2 RPL36A-HNRNPH2

Linked Data

• dbSNP Id: rs1928845685

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101412693_101412694insCTATTCTTTCCTTGTGTT , CM000685.2:g.101412693_101412694insCTATTCTTTCCTTGTGTT	GRCh38
NC_000023.10:g.100667681_100667682insCTATTCTTTCCTTGTGTT , CM000685.1:g.100667681_100667682insCTATTCTTTCCTTGTGTT	GRCh37
NC_000023.9:g.100554337_100554338insCTATTCTTTCCTTGTGTT	NCBI36
NG_007119.1:g.270_271insAACACAAGGAAAGAATAG , LRG_672:g.270_271insAACACAAGGAAAGAATAG
NG_016327.1:g.9491_9492insCTATTCTTTCCTTGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316594.6:c.705_706insCTATTCTTTCCTTGTGTT (HNRNPH2) MANE Select	ENSP00000361927.2:p.Ala235_Tyr236insLeuPhePheProCysVal
ENST00000316594.5:c.705_706insCTATTCTTTCCTTGTGTT (HNRNPH2)	ENSP00000361927.2:p.Ala235_Tyr236insLeuPhePheProCysVal
NM_001032393.2:c.705_706insCTATTCTTTCCTTGTGTT (HNRNPH2)	NP_001027565.1:p.Ala235_Tyr236insLeuPhePheProCysVal
NM_001199973.1:c.*701_*702insCTATTCTTTCCTTGTGTT (RPL36A-HNRNPH2)	NP_001186902.1:n.*701_*702insCTATTCTTTCCTTGTGTT
NM_001199974.1:c.*701_*702insCTATTCTTTCCTTGTGTT (RPL36A-HNRNPH2)	NP_001186903.1:n.*701_*702insCTATTCTTTCCTTGTGTT
NM_019597.4:c.705_706insCTATTCTTTCCTTGTGTT (HNRNPH2)	NP_062543.1:p.Ala235_Tyr236insLeuPhePheProCysVal
NM_001199973.2:c.*701_*702insCTATTCTTTCCTTGTGTT (RPL36A-HNRNPH2)	NP_001186902.2:n.*701_*702insCTATTCTTTCCTTGTGTT
NM_001199974.2:c.*701_*702insCTATTCTTTCCTTGTGTT (RPL36A-HNRNPH2)	NP_001186903.2:n.*701_*702insCTATTCTTTCCTTGTGTT
NM_019597.5:c.705_706insCTATTCTTTCCTTGTGTT (HNRNPH2) MANE Select	NP_062543.1:p.Ala235_Tyr236insLeuPhePheProCysVal
NM_001032393.3:c.705_706insCTATTCTTTCCTTGTGTT (HNRNPH2)	NP_001027565.1:p.Ala235_Tyr236insLeuPhePheProCysVal