Canonical Allele Identifier: CA797205620

Gene: WFS1

Linked Data

• dbSNP Id: rs1254677129
• gnomAD v3: 4-6300488-GCCACCTGGAGAAGGGGGGAGGGAGGA-G
• gnomAD v4: 4-6300488-GCCACCTGGAGAAGGGGGGAGGGAGGA-G
• MyVariant Identifiers: chr4:g.6302216_6302241del (hg19) ; chr4:g.6300489_6300514del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300493_6300518del , CM000666.2:g.6300493_6300518del	GRCh38
NC_000004.11:g.6302220_6302245del , CM000666.1:g.6302220_6302245del	GRCh37
NC_000004.10:g.6353121_6353146del	NCBI36
NG_011700.1:g.35644_35669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-164_898-139del	ENSP00000507852.1:n.898-164_898-139del
ENST00000683395.1:c.839-164_839-139del
ENST00000684087.1:c.862-164_862-139del	ENSP00000506978.1:n.862-164_862-139del
ENST00000506362.2:c.613-164_613-139del	ENSP00000424103.2:n.613-164_613-139del
ENST00000673642.1:c.661-304_661-279del	ENSP00000501242.1:n.661-304_661-279del
ENST00000673991.1:c.898-164_898-139del	ENSP00000501033.1:n.898-164_898-139del
ENST00000226760.5:c.862-164_862-139del MANE Select	ENSP00000226760.1:n.862-164_862-139del
ENST00000503569.5:c.862-164_862-139del	ENSP00000423337.1:n.862-164_862-139del
ENST00000506362.1:c.495-164_495-139del
ENST00000507765.1:n.1047-164_1047-139del
ENST00000513395.1:n.420-164_420-139del
NM_001145853.1:c.862-164_862-139del	NP_001139325.1:n.862-164_862-139del
NM_006005.3:c.862-164_862-139del MANE Select	NP_005996.2:n.862-164_862-139del
XM_017008586.1:c.871-164_871-139del	XP_016864075.1:n.871-164_871-139del