Canonical Allele Identifier: CA1435772977
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302575_6302577delinsCAG , CM000666.2:g.6302575_6302577delinsCAG GRCh38
NC_000004.11:g.6304302_6304304delinsCAG , CM000666.1:g.6304302_6304304delinsCAG GRCh37
NC_000004.10:g.6355203_6355205delinsCAG NCBI36
NG_011700.1:g.37726_37728delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*107_*109delinsCAG ENSP00000507852.1:n.*107_*109delinsCAG
ENST00000683395.1:c.2757_2759delinsCAG
ENST00000684087.1:c.*107_*109delinsCAG ENSP00000506978.1:n.*107_*109delinsCAG
ENST00000506362.2:c.*107_*109delinsCAG ENSP00000424103.2:n.*107_*109delinsCAG
ENST00000673991.1:c.*107_*109delinsCAG ENSP00000501033.1:n.*107_*109delinsCAG
ENST00000226760.5:c.*107_*109delinsCAG MANE Select ENSP00000226760.1:n.*107_*109delinsCAG
ENST00000503569.5:c.*107_*109delinsCAG ENSP00000423337.1:n.*107_*109delinsCAG
ENST00000507765.1:n.2965_2967delinsCAG
NM_001145853.1:c.*107_*109delinsCAG NP_001139325.1:n.*107_*109delinsCAG
NM_006005.3:c.*107_*109delinsCAG MANE Select NP_005996.2:n.*107_*109delinsCAG
XM_017008586.1:c.*107_*109delinsCAG XP_016864075.1:n.*107_*109delinsCAG