Canonical Allele Identifier: CA1435772775

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302428_6302434delinsCCTTCGA , CM000666.2:g.6302428_6302434delinsCCTTCGA	GRCh38
NC_000004.11:g.6304155_6304161delinsCCTTCGA , CM000666.1:g.6304155_6304161delinsCCTTCGA	GRCh37
NC_000004.10:g.6355056_6355062delinsCCTTCGA	NCBI36
NG_011700.1:g.37579_37585delinsCCTTCGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.2669_2675delinsCCTTCGA	ENSP00000507852.1:p.Ala890=
ENST00000683395.1:c.2610_2616delinsCCTTCGA
ENST00000684087.1:c.2633_2639delinsCCTTCGA	ENSP00000506978.1:p.Ala878=
ENST00000506362.2:c.2384_2390delinsCCTTCGA	ENSP00000424103.2:p.Ala795=
ENST00000673991.1:c.2669_2675delinsCCTTCGA	ENSP00000501033.1:p.Ala890=
ENST00000226760.5:c.2633_2639delinsCCTTCGA MANE Select	ENSP00000226760.1:p.Ala878=
ENST00000503569.5:c.2633_2639delinsCCTTCGA	ENSP00000423337.1:p.Ala878=
ENST00000507765.1:n.2818_2824delinsCCTTCGA
NM_001145853.1:c.2633_2639delinsCCTTCGA	NP_001139325.1:p.Ala878=
NM_006005.3:c.2633_2639delinsCCTTCGA MANE Select	NP_005996.2:p.Ala878=
XM_017008586.1:c.2642_2648delinsCCTTCGA	XP_016864075.1:p.Ala881=