Canonical Allele Identifier: CA797205708

Gene: WFS1

Linked Data

• dbSNP Id: rs1278966420
• MyVariant Identifiers: chr4:g.6302271_6302286del (hg19) ; chr4:g.6300544_6300559del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300545_6300560del , CM000666.2:g.6300545_6300560del	GRCh38
NC_000004.11:g.6302272_6302287del , CM000666.1:g.6302272_6302287del	GRCh37
NC_000004.10:g.6353173_6353188del	NCBI36
NG_011700.1:g.35696_35711del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-112_898-97del	ENSP00000507852.1:n.898-112_898-97del
ENST00000683395.1:c.839-112_839-97del
ENST00000684087.1:c.862-112_862-97del	ENSP00000506978.1:n.862-112_862-97del
ENST00000506362.2:c.613-112_613-97del	ENSP00000424103.2:n.613-112_613-97del
ENST00000673642.1:c.661-252_661-237del	ENSP00000501242.1:n.661-252_661-237del
ENST00000673991.1:c.898-112_898-97del	ENSP00000501033.1:n.898-112_898-97del
ENST00000226760.5:c.862-112_862-97del MANE Select	ENSP00000226760.1:n.862-112_862-97del
ENST00000503569.5:c.862-112_862-97del	ENSP00000423337.1:n.862-112_862-97del
ENST00000506362.1:c.495-112_495-97del
ENST00000507765.1:n.1047-112_1047-97del
ENST00000513395.1:n.420-112_420-97del
NM_001145853.1:c.862-112_862-97del	NP_001139325.1:n.862-112_862-97del
NM_006005.3:c.862-112_862-97del MANE Select	NP_005996.2:n.862-112_862-97del
XM_017008586.1:c.871-112_871-97del	XP_016864075.1:n.871-112_871-97del