Canonical Allele Identifier: CA40505029

Gene: HNRNPU

Linked Data

• ClinVar Variation Id: 1161846
• ClinVar RCV Id: RCV002564179
• dbSNP Id: rs759371036
• gnomAD v2: 1-245027007-G-A
• gnomAD v3: 1-244863705-G-A
• gnomAD v4: 1-244863705-G-A
• MyVariant Identifiers: chr1:g.245027007G>A (hg19) ; chr1:g.244863705G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863705G>A , CM000663.2:g.244863705G>A	GRCh38
NC_000001.10:g.245027007G>A , CM000663.1:g.245027007G>A	GRCh37
NC_000001.9:g.243093630G>A	NCBI36
NG_042184.1:g.5821C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.281C>T
ENST00000283179.14:c.603C>T	ENSP00000283179.10:p.Pro201=
ENST00000444376.7:c.603C>T	ENSP00000393151.2:p.Pro201=
ENST00000476241.2:n.788C>T
ENST00000638475.1:c.387C>T	ENSP00000491305.1:p.Pro129=
ENST00000638952.1:n.834C>T
ENST00000640218.2:c.603C>T MANE Select	ENSP00000491215.1:p.Pro201=
ENST00000640306.1:c.603C>T	ENSP00000491685.1:p.Pro201=
ENST00000640440.1:c.303C>T	ENSP00000491263.1:p.Pro101=
ENST00000649899.1:n.827C>T
ENST00000283179.13:c.603C>T	ENSP00000283179.9:p.Pro201=
ENST00000444376.6:c.603C>T	ENSP00000393151.2:p.Pro201=
ENST00000476241.1:n.787C>T
NM_004501.3:c.603C>T	NP_004492.2:p.Pro201=
NM_031844.2:c.603C>T	NP_114032.2:p.Pro201=
NM_031844.3:c.603C>T MANE Select	NP_114032.2:p.Pro201=