Canonical Allele Identifier: CA345497441

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027315G>T (hg19) ; chr1:g.244864013G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864013G>T , CM000663.2:g.244864013G>T	GRCh38
NC_000001.10:g.245027315G>T , CM000663.1:g.245027315G>T	GRCh37
NC_000001.9:g.243093938G>T	NCBI36
NG_042184.1:g.5513C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.295C>A	ENSP00000283179.10:p.Leu99Met
ENST00000444376.7:c.295C>A	ENSP00000393151.2:p.Leu99Met
ENST00000476241.2:n.480C>A
ENST00000638475.1:c.79C>A	ENSP00000491305.1:p.Leu27Met
ENST00000638952.1:n.526C>A
ENST00000640218.2:c.295C>A MANE Select	ENSP00000491215.1:p.Leu99Met
ENST00000640306.1:c.295C>A	ENSP00000491685.1:p.Leu99Met
ENST00000649899.1:n.519C>A
ENST00000283179.13:c.295C>A	ENSP00000283179.9:p.Leu99Met
ENST00000444376.6:c.295C>A	ENSP00000393151.2:p.Leu99Met
ENST00000476241.1:n.479C>A
NM_004501.3:c.295C>A	NP_004492.2:p.Leu99Met
NM_031844.2:c.295C>A	NP_114032.2:p.Leu99Met
NM_031844.3:c.295C>A MANE Select	NP_114032.2:p.Leu99Met