Canonical Allele Identifier: CA2669843622

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302606-G-GCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302606_6302607insCAA , CM000666.2:g.6302606_6302607insCAA	GRCh38
NC_000004.11:g.6304333_6304334insCAA , CM000666.1:g.6304333_6304334insCAA	GRCh37
NC_000004.10:g.6355234_6355235insCAA	NCBI36
NG_011700.1:g.37757_37758insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*138_*139insCAA	ENSP00000507852.1:n.*138_*139insCAA
ENST00000683395.1:c.2788_2789insCAA
ENST00000684087.1:c.*138_*139insCAA	ENSP00000506978.1:n.*138_*139insCAA
ENST00000506362.2:c.*138_*139insCAA	ENSP00000424103.2:n.*138_*139insCAA
ENST00000673991.1:c.*138_*139insCAA	ENSP00000501033.1:n.*138_*139insCAA
ENST00000226760.5:c.*138_*139insCAA MANE Select	ENSP00000226760.1:n.*138_*139insCAA
ENST00000503569.5:c.*138_*139insCAA	ENSP00000423337.1:n.*138_*139insCAA
ENST00000507765.1:n.2996_2997insCAA
NM_001145853.1:c.*138_*139insCAA	NP_001139325.1:n.*138_*139insCAA
NM_006005.3:c.*138_*139insCAA MANE Select	NP_005996.2:n.*138_*139insCAA
XM_017008586.1:c.*138_*139insCAA	XP_016864075.1:n.*138_*139insCAA