Canonical Allele Identifier: CA1435773726

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301483_6301489delinsACTTCCT , CM000666.2:g.6301483_6301489delinsACTTCCT	GRCh38
NC_000004.11:g.6303210_6303216delinsACTTCCT , CM000666.1:g.6303210_6303216delinsACTTCCT	GRCh37
NC_000004.10:g.6354111_6354117delinsACTTCCT	NCBI36
NG_011700.1:g.36634_36640delinsACTTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1724_1730delinsACTTCCT	ENSP00000507852.1:p.Tyr575=
ENST00000683395.1:c.1665_1671delinsACTTCCT
ENST00000684087.1:c.1688_1694delinsACTTCCT	ENSP00000506978.1:p.Tyr563=
ENST00000506362.2:c.1439_1445delinsACTTCCT	ENSP00000424103.2:p.Tyr480=
ENST00000673642.1:c.1347_1353delinsACTTCCT	ENSP00000501242.1:n.1347_1353delinsACTTCCT
ENST00000673991.1:c.1724_1730delinsACTTCCT	ENSP00000501033.1:p.Tyr575=
ENST00000226760.5:c.1688_1694delinsACTTCCT MANE Select	ENSP00000226760.1:p.Tyr563=
ENST00000503569.5:c.1688_1694delinsACTTCCT	ENSP00000423337.1:p.Tyr563=
ENST00000507765.1:n.1873_1879delinsACTTCCT
NM_001145853.1:c.1688_1694delinsACTTCCT	NP_001139325.1:p.Tyr563=
NM_006005.3:c.1688_1694delinsACTTCCT MANE Select	NP_005996.2:p.Tyr563=
XM_017008586.1:c.1697_1703delinsACTTCCT	XP_016864075.1:p.Tyr566=