Canonical Allele Identifier: CA338613916
Gene: SPEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15930594A>T , CM000663.2:g.15930594A>T GRCh38
NC_000001.10:g.16257089A>T , CM000663.1:g.16257089A>T GRCh37
NC_000001.9:g.16129676A>T NCBI36
NG_050663.1:g.87731A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000438066.2:c.*5205A>T ENSP00000388021.2:n.*5205A>T
ENST00000375759.8:c.4354A>T MANE Select ENSP00000364912.3:p.Lys1452Ter
ENST00000375759.7:c.4354A>T ENSP00000364912.3:p.Lys1452Ter
NM_015001.2:c.4354A>T NP_055816.2:p.Lys1452Ter
NM_015001.3:c.4354A>T MANE Select NP_055816.2:p.Lys1452Ter