Canonical Allele Identifier: CA2669826265

Gene: WFS1

Linked Data

• gnomAD v4: 4-6292037-GCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCGTGCCTCCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6292038_6292111del , CM000666.2:g.6292038_6292111del	GRCh38
NC_000004.11:g.6293765_6293838del , CM000666.1:g.6293765_6293838del	GRCh37
NC_000004.10:g.6344666_6344739del	NCBI36
NG_011700.1:g.27189_27262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.712+41_712+114del	ENSP00000507852.1:n.712+41_712+114del
ENST00000683395.1:c.689+41_689+114del
ENST00000684087.1:c.712+41_712+114del	ENSP00000506978.1:n.712+41_712+114del
ENST00000506362.2:c.463+41_463+114del	ENSP00000424103.2:n.463+41_463+114del
ENST00000673642.1:c.511+41_511+114del	ENSP00000501242.1:n.511+41_511+114del
ENST00000673991.1:c.712+41_712+114del	ENSP00000501033.1:n.712+41_712+114del
ENST00000226760.5:c.712+41_712+114del MANE Select	ENSP00000226760.1:n.712+41_712+114del
ENST00000503569.5:c.712+41_712+114del	ENSP00000423337.1:n.712+41_712+114del
ENST00000506362.1:c.309+41_309+114del
ENST00000507765.1:n.897+41_897+114del
NM_001145853.1:c.712+41_712+114del	NP_001139325.1:n.712+41_712+114del
NM_006005.3:c.712+41_712+114del MANE Select	NP_005996.2:n.712+41_712+114del
XM_017008586.1:c.721+41_721+114del	XP_016864075.1:n.721+41_721+114del