Canonical Allele Identifier: CA7175409

Gene: NEMF

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.49829392C>T , CM000676.2:g.49829392C>T	GRCh38
NC_000014.8:g.50296110C>T , CM000676.1:g.50296110C>T	GRCh37
NC_000014.7:g.49365860C>T	NCBI36
NG_051075.1:g.28812G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004713.6:c.980G>A MANE Select	NP_004704.3:p.Arg327Gln
ENST00000298310.10:c.980G>A MANE Select	ENSP00000298310.5:p.Arg327Gln
NM_001301732.1:c.980G>A	NP_001288661.1:p.Arg327Gln
NM_001301732.2:c.980G>A	NP_001288661.1:p.Arg327Gln
NM_001301732.3:c.980G>A	NP_001288661.2:p.Arg327Gln
NM_004713.4:c.980G>A	NP_004704.2:p.Arg327Gln
NM_004713.5:c.980G>A	NP_004704.2:p.Arg327Gln
ENST00000298310.9:c.980G>A	ENSP00000298310.5:p.Arg327Gln
ENST00000555970.5:c.854G>A	ENSP00000452540.1:p.Arg285Gln
ENST00000556925.5:n.221G>A
ENST00000557380.5:n.784G>A
XM_005268200.3:c.338G>A	XP_005268257.1:p.Arg113Gln
XM_005268201.3:c.293G>A	XP_005268258.1:p.Arg98Gln
XM_011537316.1:c.338G>A	XP_011535618.1:p.Arg113Gln
XM_011537317.1:c.980G>A	XP_011535619.1:p.Arg327Gln
XM_011537317.3:c.980G>A	XP_011535619.1:p.Arg327Gln
XM_011537318.1:c.980G>A	XP_011535620.1:p.Arg327Gln
XM_011537318.3:c.980G>A	XP_011535620.1:p.Arg327Gln
XM_017021760.2:c.293G>A	XP_016877249.1:p.Arg98Gln
XM_017021761.1:c.293G>A	XP_016877250.1:p.Arg98Gln
XR_001750595.2:n.1063G>A
XR_943556.1:n.1272G>A
XR_943557.1:n.1272G>A
XR_943557.3:n.1063G>A