Canonical Allele Identifier: CA345496799

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027105G>A (hg19) ; chr1:g.244863803G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863803G>A , CM000663.2:g.244863803G>A	GRCh38
NC_000001.10:g.245027105G>A , CM000663.1:g.245027105G>A	GRCh37
NC_000001.9:g.243093728G>A	NCBI36
NG_042184.1:g.5723C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.183C>T
ENST00000283179.14:c.505C>T	ENSP00000283179.10:p.Gln169Ter
ENST00000444376.7:c.505C>T	ENSP00000393151.2:p.Gln169Ter
ENST00000476241.2:n.690C>T
ENST00000638475.1:c.289C>T	ENSP00000491305.1:p.Gln97Ter
ENST00000638952.1:n.736C>T
ENST00000640218.2:c.505C>T MANE Select	ENSP00000491215.1:p.Gln169Ter
ENST00000640306.1:c.505C>T	ENSP00000491685.1:p.Gln169Ter
ENST00000640440.1:c.205C>T	ENSP00000491263.1:p.Gln69Ter
ENST00000649899.1:n.729C>T
ENST00000283179.13:c.505C>T	ENSP00000283179.9:p.Gln169Ter
ENST00000444376.6:c.505C>T	ENSP00000393151.2:p.Gln169Ter
ENST00000476241.1:n.689C>T
NM_004501.3:c.505C>T	NP_004492.2:p.Gln169Ter
NM_031844.2:c.505C>T	NP_114032.2:p.Gln169Ter
NM_031844.3:c.505C>T MANE Select	NP_114032.2:p.Gln169Ter