Canonical Allele Identifier: CA2760271243
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302474_6302476del , CM000666.2:g.6302474_6302476del GRCh38
NC_000004.11:g.6304201_6304203del , CM000666.1:g.6304201_6304203del GRCh37
NC_000004.10:g.6355102_6355104del NCBI36
NG_011700.1:g.37625_37627del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*6_*8del ENSP00000507852.1:n.*6_*8del
ENST00000683395.1:c.2656_2658del
ENST00000684087.1:c.*6_*8del ENSP00000506978.1:n.*6_*8del
ENST00000506362.2:c.*6_*8del ENSP00000424103.2:n.*6_*8del
ENST00000673991.1:c.*6_*8del ENSP00000501033.1:n.*6_*8del
ENST00000226760.5:c.*6_*8del MANE Select ENSP00000226760.1:n.*6_*8del
ENST00000503569.5:c.*6_*8del ENSP00000423337.1:n.*6_*8del
ENST00000507765.1:n.2864_2866del
NM_001145853.1:c.*6_*8del NP_001139325.1:n.*6_*8del
NM_006005.3:c.*6_*8del MANE Select NP_005996.2:n.*6_*8del
XM_017008586.1:c.*6_*8del XP_016864075.1:n.*6_*8del