Canonical Allele Identifier: CA1435768929

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291886_6291890delinsTCTGA , CM000666.2:g.6291886_6291890delinsTCTGA	GRCh38
NC_000004.11:g.6293613_6293617delinsTCTGA , CM000666.1:g.6293613_6293617delinsTCTGA	GRCh37
NC_000004.10:g.6344514_6344518delinsTCTGA	NCBI36
NG_011700.1:g.27037_27041delinsTCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.632-31_632-27delinsTCTGA	ENSP00000507852.1:n.632-31_632-27delinsTCTGA
ENST00000683395.1:c.609-31_609-27delinsTCTGA
ENST00000684087.1:c.632-31_632-27delinsTCTGA	ENSP00000506978.1:n.632-31_632-27delinsTCTGA
ENST00000506362.2:c.383-31_383-27delinsTCTGA	ENSP00000424103.2:n.383-31_383-27delinsTCTGA
ENST00000673642.1:c.431-31_431-27delinsTCTGA	ENSP00000501242.1:n.431-31_431-27delinsTCTGA
ENST00000673991.1:c.632-31_632-27delinsTCTGA	ENSP00000501033.1:n.632-31_632-27delinsTCTGA
ENST00000226760.5:c.632-31_632-27delinsTCTGA MANE Select	ENSP00000226760.1:n.632-31_632-27delinsTCTGA
ENST00000503569.5:c.632-31_632-27delinsTCTGA	ENSP00000423337.1:n.632-31_632-27delinsTCTGA
ENST00000506362.1:c.229-31_229-27delinsTCTGA
ENST00000507765.1:n.817-31_817-27delinsTCTGA
NM_001145853.1:c.632-31_632-27delinsTCTGA	NP_001139325.1:n.632-31_632-27delinsTCTGA
NM_006005.3:c.632-31_632-27delinsTCTGA MANE Select	NP_005996.2:n.632-31_632-27delinsTCTGA
XM_017008586.1:c.641-31_641-27delinsTCTGA	XP_016864075.1:n.641-31_641-27delinsTCTGA