Canonical Allele Identifier: CA1155574296
Gene: SPEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15930677_15930681delinsTAAAG , CM000663.2:g.15930677_15930681delinsTAAAG GRCh38
NC_000001.10:g.16257172_16257176delinsTAAAG , CM000663.1:g.16257172_16257176delinsTAAAG GRCh37
NC_000001.9:g.16129759_16129763delinsTAAAG NCBI36
NG_050663.1:g.87814_87818delinsTAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000438066.2:c.*5288_*5292delinsTAAAG ENSP00000388021.2:n.*5288_*5292delinsTAAA...
ENST00000704274.1:c.34_38delinsTAAAG
ENST00000375759.8:c.4437_4441delinsTAAAG MANE Select ENSP00000364912.3:p.Asp1479=
ENST00000375759.7:c.4437_4441delinsTAAAG ENSP00000364912.3:p.Asp1479=
NM_015001.2:c.4437_4441delinsTAAAG NP_055816.2:p.Asp1479=
NM_015001.3:c.4437_4441delinsTAAAG MANE Select NP_055816.2:p.Asp1479=