Canonical Allele Identifier: CA338973237

Gene: HNRNPR

Linked Data

• ClinVar Variation Id: 3106439
• ClinVar RCV Id: RCV004399829
• gnomAD v4: 1-23340914-G-A
• MyVariant Identifiers: chr1:g.23667407G>A (hg19) ; chr1:g.23340914G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23340914G>A , CM000663.2:g.23340914G>A	GRCh38
NC_000001.10:g.23667407G>A , CM000663.1:g.23667407G>A	GRCh37
NC_000001.9:g.23539994G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463552.6:c.95C>T	ENSP00000502509.2:p.Thr32Ile
ENST00000470941.6:c.95C>T	ENSP00000502234.2:p.Thr32Ile
ENST00000476451.3:c.-247-2306C>T	ENSP00000502301.2:n.-247-2306C>T
ENST00000302271.11:c.95C>T MANE Select	ENSP00000304405.6:p.Thr32Ile
ENST00000476451.2:c.-247-2306C>T	ENSP00000502301.1:n.-247-2306C>T
ENST00000675048.1:c.95C>T	ENSP00000502029.1:p.Thr32Ile
ENST00000302271.10:c.95C>T	ENSP00000304405.6:p.Thr32Ile
ENST00000374612.5:c.95C>T	ENSP00000363741.1:p.Thr32Ile
ENST00000374616.7:c.95C>T	ENSP00000363745.3:p.Thr32Ile
ENST00000427764.3:c.95C>T	ENSP00000392799.2:p.Thr32Ile
ENST00000478691.5:c.-146-2306C>T	ENSP00000474437.1:n.-146-2306C>T
ENST00000490652.1:n.211C>T
ENST00000606561.5:c.-146-2306C>T	ENSP00000475760.1:n.-146-2306C>T
NM_001102397.2:c.-146-2306C>T	NP_001095867.1:n.-146-2306C>T
NM_001102398.2:c.95C>T	NP_001095868.1:p.Thr32Ile
NM_001102399.2:c.-146-2306C>T	NP_001095869.1:n.-146-2306C>T
NM_001297620.1:c.95C>T	NP_001284549.1:p.Thr32Ile
NM_001297621.1:c.-146-2306C>T	NP_001284550.1:n.-146-2306C>T
NM_001297622.1:c.-146-2306C>T	NP_001284551.1:n.-146-2306C>T
NM_005826.4:c.95C>T	NP_005817.1:p.Thr32Ile
XM_005245711.3:c.95C>T	XP_005245768.1:p.Thr32Ile
XM_011540471.1:c.95C>T	XP_011538773.1:p.Thr32Ile
XM_011540472.1:c.95C>T	XP_011538774.1:p.Thr32Ile
XM_011540473.1:c.95C>T	XP_011538775.1:p.Thr32Ile
XM_011540474.1:c.95C>T	XP_011538776.1:p.Thr32Ile
XM_011540475.1:c.95C>T	XP_011538777.1:p.Thr32Ile
XM_011540476.1:c.-146-2306C>T	XP_011538778.1:n.-146-2306C>T
XM_011540477.1:c.-146-2306C>T	XP_011538779.1:n.-146-2306C>T
XM_005245711.5:c.95C>T	XP_005245768.1:p.Thr32Ile
XM_011540471.3:c.95C>T	XP_011538773.1:p.Thr32Ile
XM_011540472.3:c.95C>T	XP_011538774.1:p.Thr32Ile
XM_011540474.3:c.95C>T	XP_011538776.1:p.Thr32Ile
XM_011540475.3:c.95C>T	XP_011538777.1:p.Thr32Ile
XM_011540476.3:c.-146-2306C>T	XP_011538778.1:n.-146-2306C>T
XM_011540477.3:c.-146-2306C>T	XP_011538779.1:n.-146-2306C>T
XM_017000008.2:c.95C>T	XP_016855497.1:p.Thr32Ile
XM_017000009.2:c.95C>T	XP_016855498.1:p.Thr32Ile
XM_017000010.2:c.95C>T	XP_016855499.1:p.Thr32Ile
NM_005826.5:c.95C>T MANE Select	NP_005817.1:p.Thr32Ile
NM_001102397.3:c.-146-2306C>T	NP_001095867.1:n.-146-2306C>T
NM_001102398.3:c.95C>T	NP_001095868.1:p.Thr32Ile
NM_001102399.3:c.-146-2306C>T	NP_001095869.1:n.-146-2306C>T
NM_001297620.2:c.95C>T	NP_001284549.1:p.Thr32Ile
NM_001297621.2:c.-146-2306C>T	NP_001284550.1:n.-146-2306C>T
NM_001297622.2:c.-146-2306C>T	NP_001284551.1:n.-146-2306C>T