Canonical Allele Identifier: CA2985111

Gene: HNRNPDL

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.82429446C>A , CM000666.2:g.82429446C>A	GRCh38
NC_000004.11:g.83350599C>A , CM000666.1:g.83350599C>A	GRCh37
NC_000004.10:g.83569623C>A	NCBI36
NG_029681.1:g.5780G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_031372.4:c.245G>T MANE Select	NP_112740.1:p.Arg82Leu
ENST00000295470.10:c.245G>T MANE Select	ENSP00000295470.5:p.Arg82Leu
NM_001207000.1:c.245G>T	NP_001193929.1:p.Arg82Leu
NM_031372.3:c.245G>T	NP_112740.1:p.Arg82Leu
NR_003249.2:n.780G>T
ENST00000295470.9:c.245G>T	ENSP00000295470.5:p.Arg82Leu
ENST00000349655.8:c.-113G>T	ENSP00000338552.5:n.-113G>T
ENST00000502762.4:c.245G>T	ENSP00000422040.1:p.Arg82Leu
ENST00000614627.4:c.245G>T	ENSP00000478723.1:p.Arg82Leu
ENST00000621267.4:c.245G>T	ENSP00000483254.1:p.Arg82Leu
ENST00000630114.2:c.-79-34G>T	ENSP00000486452.1:n.-79-34G>T
ENST00000630827.1:c.-79-34G>T	ENSP00000485954.1:n.-79-34G>T