Canonical Allele Identifier: CA1155574166
Gene: SPEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15930587A= , CM000663.2:g.15930587A= GRCh38
NC_000001.10:g.16257082A= , CM000663.1:g.16257082A= GRCh37
NC_000001.9:g.16129669A= NCBI36
NG_050663.1:g.87724A=

Transcript Alleles

HGVS Amino-acid change
ENST00000438066.2:c.*5198A= ENSP00000388021.2:n.*5198A=
ENST00000375759.8:c.4347A= MANE Select ENSP00000364912.3:p.Glu1449=
ENST00000375759.7:c.4347A= ENSP00000364912.3:p.Glu1449=
NM_015001.2:c.4347A= NP_055816.2:p.Glu1449=
NM_015001.3:c.4347A= MANE Select NP_055816.2:p.Glu1449=