Canonical Allele Identifier: CA2839724
Community Standard Title: NM_006005.3(WFS1):c.2406C>G (p.Ile802Met)
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302201C>G , CM000666.2:g.6302201C>G GRCh38
NC_000004.11:g.6303928C>G , CM000666.1:g.6303928C>G GRCh37
NC_000004.10:g.6354829C>G NCBI36
NG_011700.1:g.37352C>G

Transcript Alleles

HGVS Amino-acid Change
NM_006005.3:c.2406C>G MANE Select NP_005996.2:p.Ile802Met
ENST00000226760.5:c.2406C>G MANE Select ENSP00000226760.1:p.Ile802Met
NM_001145853.1:c.2406C>G NP_001139325.1:p.Ile802Met
ENST00000503569.5:c.2406C>G ENSP00000423337.1:p.Ile802Met
ENST00000506362.2:c.2157C>G ENSP00000424103.2:p.Ile719Met
ENST00000507765.1:n.2591C>G
ENST00000673991.1:c.2442C>G ENSP00000501033.1:p.Ile814Met
ENST00000682275.1:c.2442C>G ENSP00000507852.1:p.Ile814Met
ENST00000683395.1:c.2383C>G
ENST00000684087.1:c.2406C>G ENSP00000506978.1:p.Ile802Met
XM_017008586.1:c.2415C>G XP_016864075.1:p.Ile805Met