Canonical Allele Identifier: CA438211044

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6293654G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291927G>C , CM000666.2:g.6291927G>C	GRCh38
NC_000004.11:g.6293654G>C , CM000666.1:g.6293654G>C	GRCh37
NC_000004.10:g.6344555G>C	NCBI36
NG_011700.1:g.27078G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.642G>C	ENSP00000507852.1:p.Ala214=
ENST00000683395.1:c.619G>C
ENST00000684087.1:c.642G>C	ENSP00000506978.1:p.Ala214=
ENST00000506362.2:c.393G>C	ENSP00000424103.2:p.Ala131=
ENST00000673642.1:c.441G>C	ENSP00000501242.1:p.Ala147=
ENST00000673991.1:c.642G>C	ENSP00000501033.1:p.Ala214=
ENST00000226760.5:c.642G>C MANE Select	ENSP00000226760.1:p.Ala214=
ENST00000503569.5:c.642G>C	ENSP00000423337.1:p.Ala214=
ENST00000506362.1:c.239G>C
ENST00000507765.1:n.827G>C
NM_001145853.1:c.642G>C	NP_001139325.1:p.Ala214=
NM_006005.3:c.642G>C MANE Select	NP_005996.2:p.Ala214=
XM_017008586.1:c.651G>C	XP_016864075.1:p.Ala217=