Canonical Allele Identifier: CA1435768742
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291537_6291542delinsGAACCT , CM000666.2:g.6291537_6291542delinsGAACCT GRCh38
NC_000004.11:g.6293264_6293269delinsGAACCT , CM000666.1:g.6293264_6293269delinsGAACCT GRCh37
NC_000004.10:g.6344165_6344170delinsGAACCT NCBI36
NG_011700.1:g.26688_26693delinsGAACCT

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.631+170_631+175delinsGAACCT ENSP00000507852.1:n.631+170_631+175delins...
ENST00000683395.1:c.608+183_608+188delinsGAACCT
ENST00000684087.1:c.631+170_631+175delinsGAACCT ENSP00000506978.1:n.631+170_631+175delins...
ENST00000684700.1:c.*96_*101delinsGAACCT ENSP00000507806.1:n.*96_*101delinsGAACCT
ENST00000506362.2:c.382+170_382+175delinsGAACCT ENSP00000424103.2:n.382+170_382+175delins...
ENST00000673642.1:c.430+170_430+175delinsGAACCT ENSP00000501242.1:n.430+170_430+175delins...
ENST00000673991.1:c.631+170_631+175delinsGAACCT ENSP00000501033.1:n.631+170_631+175delins...
ENST00000226760.5:c.631+170_631+175delinsGAACCT MANE Select ENSP00000226760.1:n.631+170_631+175delins...
ENST00000503569.5:c.631+170_631+175delinsGAACCT ENSP00000423337.1:n.631+170_631+175delins...
ENST00000506362.1:c.228+170_228+175delinsGAACCT
ENST00000507765.1:n.816+170_816+175delinsGAACCT
NM_001145853.1:c.631+170_631+175delinsGAACCT NP_001139325.1:n.631+170_631+175delinsGAA...
NM_006005.3:c.631+170_631+175delinsGAACCT MANE Select NP_005996.2:n.631+170_631+175delinsGAACCT...
XM_017008586.1:c.640+170_640+175delinsGAACCT XP_016864075.1:n.640+170_640+175delinsGAA...