Canonical Allele Identifier: CA797211751
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1319337577

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302559_6302577del , CM000666.2:g.6302559_6302577del GRCh38
NC_000004.11:g.6304286_6304304del , CM000666.1:g.6304286_6304304del GRCh37
NC_000004.10:g.6355187_6355205del NCBI36
NG_011700.1:g.37710_37728del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*91_*109del ENSP00000507852.1:n.*91_*109del
ENST00000683395.1:c.2741_2759del
ENST00000684087.1:c.*91_*109del ENSP00000506978.1:n.*91_*109del
ENST00000506362.2:c.*91_*109del ENSP00000424103.2:n.*91_*109del
ENST00000673991.1:c.*91_*109del ENSP00000501033.1:n.*91_*109del
ENST00000226760.5:c.*91_*109del MANE Select ENSP00000226760.1:n.*91_*109del
ENST00000503569.5:c.*91_*109del ENSP00000423337.1:n.*91_*109del
ENST00000507765.1:n.2949_2967del
NM_001145853.1:c.*91_*109del NP_001139325.1:n.*91_*109del
NM_006005.3:c.*91_*109del MANE Select NP_005996.2:n.*91_*109del
XM_017008586.1:c.*91_*109del XP_016864075.1:n.*91_*109del