Canonical Allele Identifier: CA2669843017

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300511-A-AGGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300512_6300515dup , CM000666.2:g.6300512_6300515dup	GRCh38
NC_000004.11:g.6302239_6302242dup , CM000666.1:g.6302239_6302242dup	GRCh37
NC_000004.10:g.6353140_6353143dup	NCBI36
NG_011700.1:g.35663_35666dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-145_898-142dup	ENSP00000507852.1:n.898-145_898-142dup
ENST00000683395.1:c.839-145_839-142dup
ENST00000684087.1:c.862-145_862-142dup	ENSP00000506978.1:n.862-145_862-142dup
ENST00000506362.2:c.613-145_613-142dup	ENSP00000424103.2:n.613-145_613-142dup
ENST00000673642.1:c.661-285_661-282dup	ENSP00000501242.1:n.661-285_661-282dup
ENST00000673991.1:c.898-145_898-142dup	ENSP00000501033.1:n.898-145_898-142dup
ENST00000226760.5:c.862-145_862-142dup MANE Select	ENSP00000226760.1:n.862-145_862-142dup
ENST00000503569.5:c.862-145_862-142dup	ENSP00000423337.1:n.862-145_862-142dup
ENST00000506362.1:c.495-145_495-142dup
ENST00000507765.1:n.1047-145_1047-142dup
ENST00000513395.1:n.420-145_420-142dup
NM_001145853.1:c.862-145_862-142dup	NP_001139325.1:n.862-145_862-142dup
NM_006005.3:c.862-145_862-142dup MANE Select	NP_005996.2:n.862-145_862-142dup
XM_017008586.1:c.871-145_871-142dup	XP_016864075.1:n.871-145_871-142dup