Canonical Allele Identifier: CA338613851
Gene: SPEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15930582C>G , CM000663.2:g.15930582C>G GRCh38
NC_000001.10:g.16257077C>G , CM000663.1:g.16257077C>G GRCh37
NC_000001.9:g.16129664C>G NCBI36
NG_050663.1:g.87719C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000438066.2:c.*5193C>G ENSP00000388021.2:n.*5193C>G
ENST00000375759.8:c.4342C>G MANE Select ENSP00000364912.3:p.Leu1448Val
ENST00000375759.7:c.4342C>G ENSP00000364912.3:p.Leu1448Val
NM_015001.2:c.4342C>G NP_055816.2:p.Leu1448Val
NM_015001.3:c.4342C>G MANE Select NP_055816.2:p.Leu1448Val