Canonical Allele Identifier: CA2669843693
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302660_6302669del , CM000666.2:g.6302660_6302669del GRCh38
NC_000004.11:g.6304387_6304396del , CM000666.1:g.6304387_6304396del GRCh37
NC_000004.10:g.6355288_6355297del NCBI36
NG_011700.1:g.37811_37820del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*192_*201del ENSP00000507852.1:n.*192_*201del
ENST00000683395.1:c.2842_2851del
ENST00000684087.1:c.*192_*201del ENSP00000506978.1:n.*192_*201del
ENST00000506362.2:c.*192_*201del ENSP00000424103.2:n.*192_*201del
ENST00000673991.1:c.*192_*201del ENSP00000501033.1:n.*192_*201del
ENST00000226760.5:c.*192_*201del MANE Select ENSP00000226760.1:n.*192_*201del
ENST00000503569.5:c.*192_*201del ENSP00000423337.1:n.*192_*201del
ENST00000507765.1:n.3050_3059del
NM_001145853.1:c.*192_*201del NP_001139325.1:n.*192_*201del
NM_006005.3:c.*192_*201del MANE Select NP_005996.2:n.*192_*201del
XM_017008586.1:c.*192_*201del XP_016864075.1:n.*192_*201del