Canonical Allele Identifier: CA2984778

Gene: HNRNPDL

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.82426558C>G , CM000666.2:g.82426558C>G	GRCh38
NC_000004.11:g.83347711C>G , CM000666.1:g.83347711C>G	GRCh37
NC_000004.10:g.83566735C>G	NCBI36
NG_029681.1:g.8668G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_031372.4:c.1097G>C MANE Select	NP_112740.1:p.Gly366Ala
ENST00000295470.10:c.1097G>C MANE Select	ENSP00000295470.5:p.Gly366Ala
NM_001207000.1:c.1022-429G>C	NP_001193929.1:n.1022-429G>C
NM_031372.3:c.1097G>C	NP_112740.1:p.Gly366Ala
NR_003249.2:n.1632G>C
ENST00000295470.9:c.1097G>C	ENSP00000295470.5:p.Gly366Ala
ENST00000349655.8:c.740G>C	ENSP00000338552.5:p.Gly247Ala
ENST00000502762.4:c.1097G>C	ENSP00000422040.1:p.Gly366Ala
ENST00000507721.5:c.740G>C	ENSP00000480156.1:p.Gly247Ala
ENST00000514511.1:c.*235G>C	ENSP00000478269.1:n.*235G>C
ENST00000602300.5:c.740G>C	ENSP00000473677.1:p.Gly247Ala
ENST00000614627.4:c.1022-429G>C	ENSP00000478723.1:n.1022-429G>C
ENST00000621267.4:c.1097G>C	ENSP00000483254.1:p.Gly366Ala
ENST00000630114.2:c.740G>C	ENSP00000486452.1:p.Gly247Ala
ENST00000630827.1:c.740G>C	ENSP00000485954.1:p.Gly247Ala