Canonical Allele Identifier: CA1231007573

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864053_244864059delinsCTCTTCA , CM000663.2:g.244864053_244864059delinsCTCTTCA	GRCh38
NC_000001.10:g.245027355_245027361delinsCTCTTCA , CM000663.1:g.245027355_245027361delinsCTCTTCA	GRCh37
NC_000001.9:g.243093978_243093984delinsCTCTTCA	NCBI36
NG_042184.1:g.5467_5473delinsTGAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.249_255delinsTGAAGAG	ENSP00000283179.10:p.Asp83=
ENST00000444376.7:c.249_255delinsTGAAGAG	ENSP00000393151.2:p.Asp83=
ENST00000476241.2:n.434_440delinsTGAAGAG
ENST00000638475.1:c.33_39delinsTGAAGAG	ENSP00000491305.1:p.Asp11=
ENST00000638952.1:n.480_486delinsTGAAGAG
ENST00000640218.2:c.249_255delinsTGAAGAG MANE Select	ENSP00000491215.1:p.Asp83=
ENST00000640306.1:c.249_255delinsTGAAGAG	ENSP00000491685.1:p.Asp83=
ENST00000649899.1:n.473_479delinsTGAAGAG
ENST00000283179.13:c.249_255delinsTGAAGAG	ENSP00000283179.9:p.Asp83=
ENST00000444376.6:c.249_255delinsTGAAGAG	ENSP00000393151.2:p.Asp83=
ENST00000476241.1:n.433_439delinsTGAAGAG
NM_004501.3:c.249_255delinsTGAAGAG	NP_004492.2:p.Asp83=
NM_031844.2:c.249_255delinsTGAAGAG	NP_114032.2:p.Asp83=
NM_031844.3:c.249_255delinsTGAAGAG MANE Select	NP_114032.2:p.Asp83=