Canonical Allele Identifier: CA797205641

Gene: WFS1

Linked Data

• dbSNP Id: rs1466378161
• MyVariant Identifiers: chr4:g.6302229_6302230insGGGGA (hg19) ; chr4:g.6300502_6300503insGGGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300506_6300510dup , CM000666.2:g.6300506_6300510dup	GRCh38
NC_000004.11:g.6302233_6302237dup , CM000666.1:g.6302233_6302237dup	GRCh37
NC_000004.10:g.6353134_6353138dup	NCBI36
NG_011700.1:g.35657_35661dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-151_898-147dup	ENSP00000507852.1:n.898-151_898-147dup
ENST00000683395.1:c.839-151_839-147dup
ENST00000684087.1:c.862-151_862-147dup	ENSP00000506978.1:n.862-151_862-147dup
ENST00000506362.2:c.613-151_613-147dup	ENSP00000424103.2:n.613-151_613-147dup
ENST00000673642.1:c.661-291_661-287dup	ENSP00000501242.1:n.661-291_661-287dup
ENST00000673991.1:c.898-151_898-147dup	ENSP00000501033.1:n.898-151_898-147dup
ENST00000226760.5:c.862-151_862-147dup MANE Select	ENSP00000226760.1:n.862-151_862-147dup
ENST00000503569.5:c.862-151_862-147dup	ENSP00000423337.1:n.862-151_862-147dup
ENST00000506362.1:c.495-151_495-147dup
ENST00000507765.1:n.1047-151_1047-147dup
ENST00000513395.1:n.420-151_420-147dup
NM_001145853.1:c.862-151_862-147dup	NP_001139325.1:n.862-151_862-147dup
NM_006005.3:c.862-151_862-147dup MANE Select	NP_005996.2:n.862-151_862-147dup
XM_017008586.1:c.871-151_871-147dup	XP_016864075.1:n.871-151_871-147dup