Canonical Allele Identifier: CA658764575

Gene: HNRNPU

Linked Data

• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863909_244863915del , CM000663.2:g.244863909_244863915del	GRCh38
NC_000001.10:g.245027211_245027217del , CM000663.1:g.245027211_245027217del	GRCh37
NC_000001.9:g.243093834_243093840del	NCBI36
NG_042184.1:g.5613_5619del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.73_79del
ENST00000283179.14:c.395_401del	ENSP00000283179.10:p.Asn132ThrfsTer?
ENST00000444376.7:c.395_401del	ENSP00000393151.2:p.Asn132ThrfsTer?
ENST00000476241.2:n.580_586del
ENST00000638475.1:c.179_185del	ENSP00000491305.1:p.Asn60ThrfsTer?
ENST00000638952.1:n.626_632del
ENST00000640218.2:c.395_401del MANE Select	ENSP00000491215.1:p.Asn132ThrfsTer?
ENST00000640306.1:c.395_401del	ENSP00000491685.1:p.Asn132ThrfsTer?
ENST00000640440.1:c.95_101del	ENSP00000491263.1:p.Asn32ThrfsTer?
ENST00000649899.1:n.619_625del
ENST00000283179.13:c.395_401del	ENSP00000283179.9:p.Asn132ThrfsTer?
ENST00000444376.6:c.395_401del	ENSP00000393151.2:p.Asn132ThrfsTer?
ENST00000476241.1:n.579_585del
NM_004501.3:c.395_401del	NP_004492.2:p.Asn132ThrfsTer?
NM_031844.2:c.395_401del	NP_114032.2:p.Asn132ThrfsTer?
NM_031844.3:c.395_401del MANE Select	NP_114032.2:p.Asn132ThrfsTer?