Canonical Allele Identifier: CA549708012

Gene: WFS1

Linked Data

• gnomAD v2: 4-6302208-G-GGGGAGGGCCACCTGGAGAAGGGGGGA
• gnomAD v3: 4-6300481-G-GGGGAGGGCCACCTGGAGAAGGGGGGA
• gnomAD v4: 4-6300481-G-GGGGAGGGCCACCTGGAGAAGGGGGGA
• MyVariant Identifiers: chr4:g.6302208_6302209insGGGAGGGCCACCTGGAGAAGGGGGGA (hg19) ; chr4:g.6300481_6300482insGGGAGGGCCACCTGGAGAAGGGGGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300488_6300513dup , CM000666.2:g.6300488_6300513dup	GRCh38
NC_000004.11:g.6302215_6302240dup , CM000666.1:g.6302215_6302240dup	GRCh37
NC_000004.10:g.6353116_6353141dup	NCBI36
NG_011700.1:g.35639_35664dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-169_898-144dup	ENSP00000507852.1:n.898-169_898-144dup
ENST00000683395.1:c.839-169_839-144dup
ENST00000684087.1:c.862-169_862-144dup	ENSP00000506978.1:n.862-169_862-144dup
ENST00000506362.2:c.613-169_613-144dup	ENSP00000424103.2:n.613-169_613-144dup
ENST00000673642.1:c.661-309_661-284dup	ENSP00000501242.1:n.661-309_661-284dup
ENST00000673991.1:c.898-169_898-144dup	ENSP00000501033.1:n.898-169_898-144dup
ENST00000226760.5:c.862-169_862-144dup MANE Select	ENSP00000226760.1:n.862-169_862-144dup
ENST00000503569.5:c.862-169_862-144dup	ENSP00000423337.1:n.862-169_862-144dup
ENST00000506362.1:c.495-169_495-144dup
ENST00000507765.1:n.1047-169_1047-144dup
ENST00000513395.1:n.420-169_420-144dup
NM_001145853.1:c.862-169_862-144dup	NP_001139325.1:n.862-169_862-144dup
NM_006005.3:c.862-169_862-144dup MANE Select	NP_005996.2:n.862-169_862-144dup
XM_017008586.1:c.871-169_871-144dup	XP_016864075.1:n.871-169_871-144dup