Canonical Allele Identifier: CA1058893149
Gene: WFS1 HGNC NCBI

Linked Data

gnomAD v3: 4-6302627-A-AT
gnomAD v4: 4-6302627-A-AT

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302627_6302628insT , CM000666.2:g.6302627_6302628insT GRCh38
NC_000004.11:g.6304354_6304355insT , CM000666.1:g.6304354_6304355insT GRCh37
NC_000004.10:g.6355255_6355256insT NCBI36
NG_011700.1:g.37778_37779insT

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.*159_*160insT ENSP00000507852.1:n.*159_*160insT
ENST00000683395.1:c.2809_2810insT
ENST00000684087.1:c.*159_*160insT ENSP00000506978.1:n.*159_*160insT
ENST00000506362.2:c.*159_*160insT ENSP00000424103.2:n.*159_*160insT
ENST00000673991.1:c.*159_*160insT ENSP00000501033.1:n.*159_*160insT
ENST00000226760.5:c.*159_*160insT MANE Select ENSP00000226760.1:n.*159_*160insT
ENST00000503569.5:c.*159_*160insT ENSP00000423337.1:n.*159_*160insT
ENST00000507765.1:n.3017_3018insT
NM_001145853.1:c.*159_*160insT NP_001139325.1:n.*159_*160insT
NM_006005.3:c.*159_*160insT MANE Select NP_005996.2:n.*159_*160insT
XM_017008586.1:c.*159_*160insT XP_016864075.1:n.*159_*160insT