Canonical Allele Identifier: CA2578035808
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302163_6302166del , CM000666.2:g.6302163_6302166del GRCh38
NC_000004.11:g.6303890_6303893del , CM000666.1:g.6303890_6303893del GRCh37
NC_000004.10:g.6354791_6354794del NCBI36
NG_011700.1:g.37314_37317del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2404_2407del ENSP00000507852.1:p.Ser802AlafsTer?
ENST00000683395.1:c.2345_2348del
ENST00000684087.1:c.2368_2371del ENSP00000506978.1:p.Ser790AlafsTer?
ENST00000506362.2:c.2119_2122del ENSP00000424103.2:p.Ser707AlafsTer?
ENST00000673991.1:c.2404_2407del ENSP00000501033.1:p.Ser802AlafsTer?
ENST00000226760.5:c.2368_2371del MANE Select ENSP00000226760.1:p.Ser790AlafsTer?
ENST00000503569.5:c.2368_2371del ENSP00000423337.1:p.Ser790AlafsTer?
ENST00000507765.1:n.2553_2556del
NM_001145853.1:c.2368_2371del NP_001139325.1:p.Ser790AlafsTer?
NM_006005.3:c.2368_2371del MANE Select NP_005996.2:p.Ser790AlafsTer?
XM_017008586.1:c.2377_2380del XP_016864075.1:p.Ser793AlafsTer?