Canonical Allele Identifier: CA2985089

Gene: HNRNPDL

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.82429417A>G , CM000666.2:g.82429417A>G	GRCh38
NC_000004.11:g.83350570A>G , CM000666.1:g.83350570A>G	GRCh37
NC_000004.10:g.83569594A>G	NCBI36
NG_029681.1:g.5809T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_031372.4:c.274T>C MANE Select	NP_112740.1:p.Ser92Pro
ENST00000295470.10:c.274T>C MANE Select	ENSP00000295470.5:p.Ser92Pro
NM_001207000.1:c.274T>C	NP_001193929.1:p.Ser92Pro
NM_031372.3:c.274T>C	NP_112740.1:p.Ser92Pro
NR_003249.2:n.809T>C
ENST00000295470.9:c.274T>C	ENSP00000295470.5:p.Ser92Pro
ENST00000349655.8:c.-84T>C	ENSP00000338552.5:n.-84T>C
ENST00000502762.4:c.274T>C	ENSP00000422040.1:p.Ser92Pro
ENST00000514511.1:c.-84T>C	ENSP00000478269.1:n.-84T>C
ENST00000602300.5:c.-84T>C	ENSP00000473677.1:n.-84T>C
ENST00000614627.4:c.274T>C	ENSP00000478723.1:p.Ser92Pro
ENST00000621267.4:c.274T>C	ENSP00000483254.1:p.Ser92Pro
ENST00000630114.2:c.-79-5T>C	ENSP00000486452.1:n.-79-5T>C
ENST00000630827.1:c.-79-5T>C	ENSP00000485954.1:n.-79-5T>C