Canonical Allele Identifier: CA338614478
Gene: SPEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15930683A>T , CM000663.2:g.15930683A>T GRCh38
NC_000001.10:g.16257178A>T , CM000663.1:g.16257178A>T GRCh37
NC_000001.9:g.16129765A>T NCBI36
NG_050663.1:g.87820A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000438066.2:c.*5294A>T ENSP00000388021.2:n.*5294A>T
ENST00000704274.1:c.40A>T
ENST00000375759.8:c.4443A>T MANE Select ENSP00000364912.3:p.Glu1481Asp
ENST00000375759.7:c.4443A>T ENSP00000364912.3:p.Glu1481Asp
NM_015001.2:c.4443A>T NP_055816.2:p.Glu1481Asp
NM_015001.3:c.4443A>T MANE Select NP_055816.2:p.Glu1481Asp