Canonical Allele Identifier: CA2651343302

Gene: HNRNPU

Linked Data

• gnomAD v4: 1-244863780-CTGCTGTTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863781_244863789del , CM000663.2:g.244863781_244863789del	GRCh38
NC_000001.10:g.245027083_245027091del , CM000663.1:g.245027083_245027091del	GRCh37
NC_000001.9:g.243093706_243093714del	NCBI36
NG_042184.1:g.5737_5745del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.197_205del
ENST00000283179.14:c.519_527del	ENSP00000283179.10:p.Gln174_Gln176del
ENST00000444376.7:c.519_527del	ENSP00000393151.2:p.Gln174_Gln176del
ENST00000476241.2:n.704_712del
ENST00000638475.1:c.303_311del	ENSP00000491305.1:p.Gln102_Gln104del
ENST00000638952.1:n.750_758del
ENST00000640218.2:c.519_527del MANE Select	ENSP00000491215.1:p.Gln174_Gln176del
ENST00000640306.1:c.519_527del	ENSP00000491685.1:p.Gln174_Gln176del
ENST00000640440.1:c.219_227del	ENSP00000491263.1:p.Gln74_Gln76del
ENST00000649899.1:n.743_751del
ENST00000283179.13:c.519_527del	ENSP00000283179.9:p.Gln174_Gln176del
ENST00000444376.6:c.519_527del	ENSP00000393151.2:p.Gln174_Gln176del
ENST00000476241.1:n.703_711del
NM_004501.3:c.519_527del	NP_004492.2:p.Gln174_Gln176del
NM_031844.2:c.519_527del	NP_114032.2:p.Gln174_Gln176del
NM_031844.3:c.519_527del MANE Select	NP_114032.2:p.Gln174_Gln176del