Canonical Allele Identifier: CA343419893

Gene: NUF2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.163345778T>C , CM000663.2:g.163345778T>C	GRCh38
NC_000001.10:g.163315568T>C , CM000663.1:g.163315568T>C	GRCh37
NC_000001.9:g.161582192T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271452.8:c.908T>C MANE Select	ENSP00000271452.3:p.Leu303Pro
ENST00000271452.7:c.908T>C	ENSP00000271452.3:p.Leu303Pro
ENST00000367900.7:c.908T>C	ENSP00000356875.3:p.Leu303Pro
ENST00000524800.5:c.807+1908T>C	ENSP00000436888.1:n.807+1908T>C
ENST00000527439.5:n.478T>C
NM_031423.3:c.908T>C	NP_113611.2:p.Leu303Pro
NM_145697.2:c.908T>C	NP_663735.2:p.Leu303Pro
XM_011510036.1:c.770T>C	XP_011508338.1:p.Leu257Pro
XM_024450112.1:c.908T>C	XP_024305880.1:p.Leu303Pro
XM_024450113.1:c.908T>C	XP_024305881.1:p.Leu303Pro
NM_145697.3:c.908T>C MANE Select	NP_663735.2:p.Leu303Pro
NM_031423.4:c.908T>C	NP_113611.2:p.Leu303Pro