Canonical Allele Identifier: CA733939004

Gene: HNRNPU

Linked Data

• dbSNP Id: rs1463934264
• MyVariant Identifiers: chr1:g.245027338_245027340del (hg19) ; chr1:g.244864036_244864038del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864038_244864040del , CM000663.2:g.244864038_244864040del	GRCh38
NC_000001.10:g.245027340_245027342del , CM000663.1:g.245027340_245027342del	GRCh37
NC_000001.9:g.243093963_243093965del	NCBI36
NG_042184.1:g.5488_5490del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.270_272del	ENSP00000283179.10:p.Glu91del
ENST00000444376.7:c.270_272del	ENSP00000393151.2:p.Glu91del
ENST00000476241.2:n.455_457del
ENST00000638475.1:c.54_56del	ENSP00000491305.1:p.Glu19del
ENST00000638952.1:n.501_503del
ENST00000640218.2:c.270_272del MANE Select	ENSP00000491215.1:p.Glu91del
ENST00000640306.1:c.270_272del	ENSP00000491685.1:p.Glu91del
ENST00000649899.1:n.494_496del
ENST00000283179.13:c.270_272del	ENSP00000283179.9:p.Glu91del
ENST00000444376.6:c.270_272del	ENSP00000393151.2:p.Glu91del
ENST00000476241.1:n.454_456del
NM_004501.3:c.270_272del	NP_004492.2:p.Glu91del
NM_031844.2:c.270_272del	NP_114032.2:p.Glu91del
NM_031844.3:c.270_272del MANE Select	NP_114032.2:p.Glu91del