Canonical Allele Identifier: CA338613905
Gene: SPEN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.16257087C>A (hg19) chr1:g.15930592C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15930592C>A , CM000663.2:g.15930592C>A GRCh38
NC_000001.10:g.16257087C>A , CM000663.1:g.16257087C>A GRCh37
NC_000001.9:g.16129674C>A NCBI36
NG_050663.1:g.87729C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000438066.2:c.*5203C>A ENSP00000388021.2:n.*5203C>A
ENST00000375759.8:c.4352C>A MANE Select ENSP00000364912.3:p.Ala1451Asp
ENST00000375759.7:c.4352C>A ENSP00000364912.3:p.Ala1451Asp
NM_015001.2:c.4352C>A NP_055816.2:p.Ala1451Asp
NM_015001.3:c.4352C>A MANE Select NP_055816.2:p.Ala1451Asp
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