Canonical Allele Identifier: CA2586968603

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863842_244863854del , CM000663.2:g.244863842_244863854del	GRCh38
NC_000001.10:g.245027144_245027156del , CM000663.1:g.245027144_245027156del	GRCh37
NC_000001.9:g.243093767_243093779del	NCBI36
NG_042184.1:g.5672_5684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.132_144del
ENST00000283179.14:c.454_466del	ENSP00000283179.10:p.Ala152ThrfsTer?
ENST00000444376.7:c.454_466del	ENSP00000393151.2:p.Ala152ThrfsTer?
ENST00000476241.2:n.639_651del
ENST00000638475.1:c.238_250del	ENSP00000491305.1:p.Ala80ThrfsTer?
ENST00000638952.1:n.685_697del
ENST00000640218.2:c.454_466del MANE Select	ENSP00000491215.1:p.Ala152ThrfsTer?
ENST00000640306.1:c.454_466del	ENSP00000491685.1:p.Ala152ThrfsTer?
ENST00000640440.1:c.154_166del	ENSP00000491263.1:p.Ala52ThrfsTer?
ENST00000649899.1:n.678_690del
ENST00000283179.13:c.454_466del	ENSP00000283179.9:p.Ala152ThrfsTer?
ENST00000444376.6:c.454_466del	ENSP00000393151.2:p.Ala152ThrfsTer?
ENST00000476241.1:n.638_650del
NM_004501.3:c.454_466del	NP_004492.2:p.Ala152ThrfsTer?
NM_031844.2:c.454_466del	NP_114032.2:p.Ala152ThrfsTer?
NM_031844.3:c.454_466del MANE Select	NP_114032.2:p.Ala152ThrfsTer?