Canonical Allele Identifier: CA1435772672
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302358_6302360delinsTCA , CM000666.2:g.6302358_6302360delinsTCA GRCh38
NC_000004.11:g.6304085_6304087delinsTCA , CM000666.1:g.6304085_6304087delinsTCA GRCh37
NC_000004.10:g.6354986_6354988delinsTCA NCBI36
NG_011700.1:g.37509_37511delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2599_2601delinsTCA ENSP00000507852.1:p.Ser867=
ENST00000683395.1:c.2540_2542delinsTCA
ENST00000684087.1:c.2563_2565delinsTCA ENSP00000506978.1:p.Ser855=
ENST00000506362.2:c.2314_2316delinsTCA ENSP00000424103.2:p.Ser772=
ENST00000673991.1:c.2599_2601delinsTCA ENSP00000501033.1:p.Ser867=
ENST00000226760.5:c.2563_2565delinsTCA MANE Select ENSP00000226760.1:p.Ser855=
ENST00000503569.5:c.2563_2565delinsTCA ENSP00000423337.1:p.Ser855=
ENST00000507765.1:n.2748_2750delinsTCA
NM_001145853.1:c.2563_2565delinsTCA NP_001139325.1:p.Ser855=
NM_006005.3:c.2563_2565delinsTCA MANE Select NP_005996.2:p.Ser855=
XM_017008586.1:c.2572_2574delinsTCA XP_016864075.1:p.Ser858=