Canonical Allele Identifier: CA345497135

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027181A>T (hg19) ; chr1:g.244863879A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863879A>T , CM000663.2:g.244863879A>T	GRCh38
NC_000001.10:g.245027181A>T , CM000663.1:g.245027181A>T	GRCh37
NC_000001.9:g.243093804A>T	NCBI36
NG_042184.1:g.5647T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.107T>A
ENST00000283179.14:c.429T>A	ENSP00000283179.10:p.Asp143Glu
ENST00000444376.7:c.429T>A	ENSP00000393151.2:p.Asp143Glu
ENST00000476241.2:n.614T>A
ENST00000638475.1:c.213T>A	ENSP00000491305.1:p.Asp71Glu
ENST00000638952.1:n.660T>A
ENST00000640218.2:c.429T>A MANE Select	ENSP00000491215.1:p.Asp143Glu
ENST00000640306.1:c.429T>A	ENSP00000491685.1:p.Asp143Glu
ENST00000640440.1:c.129T>A	ENSP00000491263.1:p.Asp43Glu
ENST00000649899.1:n.653T>A
ENST00000283179.13:c.429T>A	ENSP00000283179.9:p.Asp143Glu
ENST00000444376.6:c.429T>A	ENSP00000393151.2:p.Asp143Glu
ENST00000476241.1:n.613T>A
NM_004501.3:c.429T>A	NP_004492.2:p.Asp143Glu
NM_031844.2:c.429T>A	NP_114032.2:p.Asp143Glu
NM_031844.3:c.429T>A MANE Select	NP_114032.2:p.Asp143Glu