Canonical Allele Identifier: CA40505154

Gene: HNRNPU

Linked Data

• ClinVar Variation Id: 3026637
• ClinVar RCV Id: RCV003887030
• dbSNP Id: rs980758296
• MyVariant Identifiers: chr1:g.245027174C>G (hg19) ; chr1:g.244863872C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863872C>G , CM000663.2:g.244863872C>G	GRCh38
NC_000001.10:g.245027174C>G , CM000663.1:g.245027174C>G	GRCh37
NC_000001.9:g.243093797C>G	NCBI36
NG_042184.1:g.5654G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.114G>C
ENST00000283179.14:c.436G>C	ENSP00000283179.10:p.Gly146Arg
ENST00000444376.7:c.436G>C	ENSP00000393151.2:p.Gly146Arg
ENST00000476241.2:n.621G>C
ENST00000638475.1:c.220G>C	ENSP00000491305.1:p.Gly74Arg
ENST00000638952.1:n.667G>C
ENST00000640218.2:c.436G>C MANE Select	ENSP00000491215.1:p.Gly146Arg
ENST00000640306.1:c.436G>C	ENSP00000491685.1:p.Gly146Arg
ENST00000640440.1:c.136G>C	ENSP00000491263.1:p.Gly46Arg
ENST00000649899.1:n.660G>C
ENST00000283179.13:c.436G>C	ENSP00000283179.9:p.Gly146Arg
ENST00000444376.6:c.436G>C	ENSP00000393151.2:p.Gly146Arg
ENST00000476241.1:n.620G>C
NM_004501.3:c.436G>C	NP_004492.2:p.Gly146Arg
NM_031844.2:c.436G>C	NP_114032.2:p.Gly146Arg
NM_031844.3:c.436G>C MANE Select	NP_114032.2:p.Gly146Arg