Canonical Allele Identifier: CA345496968

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027143T>C (hg19) ; chr1:g.244863841T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863841T>C , CM000663.2:g.244863841T>C	GRCh38
NC_000001.10:g.245027143T>C , CM000663.1:g.245027143T>C	GRCh37
NC_000001.9:g.243093766T>C	NCBI36
NG_042184.1:g.5685A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.145A>G
ENST00000283179.14:c.467A>G	ENSP00000283179.10:p.Asn156Ser
ENST00000444376.7:c.467A>G	ENSP00000393151.2:p.Asn156Ser
ENST00000476241.2:n.652A>G
ENST00000638475.1:c.251A>G	ENSP00000491305.1:p.Asn84Ser
ENST00000638952.1:n.698A>G
ENST00000640218.2:c.467A>G MANE Select	ENSP00000491215.1:p.Asn156Ser
ENST00000640306.1:c.467A>G	ENSP00000491685.1:p.Asn156Ser
ENST00000640440.1:c.167A>G	ENSP00000491263.1:p.Asn56Ser
ENST00000649899.1:n.691A>G
ENST00000283179.13:c.467A>G	ENSP00000283179.9:p.Asn156Ser
ENST00000444376.6:c.467A>G	ENSP00000393151.2:p.Asn156Ser
ENST00000476241.1:n.651A>G
NM_004501.3:c.467A>G	NP_004492.2:p.Asn156Ser
NM_031844.2:c.467A>G	NP_114032.2:p.Asn156Ser
NM_031844.3:c.467A>G MANE Select	NP_114032.2:p.Asn156Ser