Canonical Allele Identifier: CA1435772084
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6300741_6300744delinsTCCA , CM000666.2:g.6300741_6300744delinsTCCA GRCh38
NC_000004.11:g.6302468_6302471delinsTCCA , CM000666.1:g.6302468_6302471delinsTCCA GRCh37
NC_000004.10:g.6353369_6353372delinsTCCA NCBI36
NG_011700.1:g.35892_35895delinsTCCA

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.982_985delinsTCCA ENSP00000507852.1:p.Ser328=
ENST00000683395.1:c.923_926delinsTCCA
ENST00000684087.1:c.946_949delinsTCCA ENSP00000506978.1:p.Ser316=
ENST00000506362.2:c.697_700delinsTCCA ENSP00000424103.2:p.Ser233=
ENST00000673642.1:c.661-56_661-53delinsTCCA ENSP00000501242.1:n.661-56_661-53delinsTC...
ENST00000673991.1:c.982_985delinsTCCA ENSP00000501033.1:p.Ser328=
ENST00000226760.5:c.946_949delinsTCCA MANE Select ENSP00000226760.1:p.Ser316=
ENST00000503569.5:c.946_949delinsTCCA ENSP00000423337.1:p.Ser316=
ENST00000506362.1:c.579_582delinsTCCA
ENST00000507765.1:n.1131_1134delinsTCCA
ENST00000513395.1:n.504_507delinsTCCA
NM_001145853.1:c.946_949delinsTCCA NP_001139325.1:p.Ser316=
NM_006005.3:c.946_949delinsTCCA MANE Select NP_005996.2:p.Ser316=
XM_017008586.1:c.955_958delinsTCCA XP_016864075.1:p.Ser319=