Canonical Allele Identifier: CA345497197

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027207C>A (hg19) ; chr1:g.244863905C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863905C>A , CM000663.2:g.244863905C>A	GRCh38
NC_000001.10:g.245027207C>A , CM000663.1:g.245027207C>A	GRCh37
NC_000001.9:g.243093830C>A	NCBI36
NG_042184.1:g.5621G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.81G>T
ENST00000283179.14:c.403G>T	ENSP00000283179.10:p.Asp135Tyr
ENST00000444376.7:c.403G>T	ENSP00000393151.2:p.Asp135Tyr
ENST00000476241.2:n.588G>T
ENST00000638475.1:c.187G>T	ENSP00000491305.1:p.Asp63Tyr
ENST00000638952.1:n.634G>T
ENST00000640218.2:c.403G>T MANE Select	ENSP00000491215.1:p.Asp135Tyr
ENST00000640306.1:c.403G>T	ENSP00000491685.1:p.Asp135Tyr
ENST00000640440.1:c.103G>T	ENSP00000491263.1:p.Asp35Tyr
ENST00000649899.1:n.627G>T
ENST00000283179.13:c.403G>T	ENSP00000283179.9:p.Asp135Tyr
ENST00000444376.6:c.403G>T	ENSP00000393151.2:p.Asp135Tyr
ENST00000476241.1:n.587G>T
NM_004501.3:c.403G>T	NP_004492.2:p.Asp135Tyr
NM_031844.2:c.403G>T	NP_114032.2:p.Asp135Tyr
NM_031844.3:c.403G>T MANE Select	NP_114032.2:p.Asp135Tyr