Canonical Allele Identifier: CA915945877

Gene: WAC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28583437dup , CM000672.2:g.28583437dup	GRCh38
NC_000010.10:g.28872366dup , CM000672.1:g.28872366dup	GRCh37
NC_000010.9:g.28912372dup	NCBI36
NG_046603.1:g.55850dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700325.1:c.301dup	ENSP00000514952.1:p.Ser101LysfsTer5
ENST00000706612.1:c.303dup	ENSP00000516469.1:p.Val102SerfsTer?
ENST00000354911.9:c.313dup MANE Select	ENSP00000346986.4:p.Ser105LysfsTer5
ENST00000414108.6:c.178dup	ENSP00000415645.2:p.Ser60LysfsTer5
ENST00000420266.6:c.*227dup	ENSP00000404758.2:n.*227dup
ENST00000428935.6:c.178dup	ENSP00000399706.3:p.Ser60LysfsTer5
ENST00000442148.6:c.178dup	ENSP00000400848.2:p.Ser60LysfsTer5
ENST00000628285.3:c.171dup	ENSP00000486994.2:p.Val58SerfsTer?
ENST00000651441.1:c.178dup	ENSP00000498450.1:p.Ser60LysfsTer5
ENST00000651598.1:c.178dup	ENSP00000498480.1:p.Ser60LysfsTer5
ENST00000651885.1:c.331dup	ENSP00000498678.1:p.Ser111LysfsTer5
ENST00000679398.1:c.178dup	ENSP00000506624.1:p.Ser60LysfsTer5
ENST00000679428.1:c.178dup	ENSP00000506445.1:p.Ser60LysfsTer5
ENST00000679570.1:c.*308dup	ENSP00000506705.1:n.*308dup
ENST00000680735.1:c.186dup	ENSP00000505513.1:p.Val63SerfsTer?
ENST00000681112.1:c.*166dup	ENSP00000505444.1:n.*166dup
ENST00000345541.6:n.111dup
ENST00000347934.8:c.313dup	ENSP00000311106.4:p.Ser105LysfsTer5
ENST00000354911.8:c.313dup	ENSP00000346986.4:p.Ser105LysfsTer5
ENST00000375646.5:c.178dup	ENSP00000364797.1:p.Ser60LysfsTer5
ENST00000375664.8:c.178dup	ENSP00000364816.3:p.Ser60LysfsTer5
ENST00000414108.5:c.178dup	ENSP00000415645.1:p.Ser60LysfsTer5
ENST00000420266.5:c.178dup	ENSP00000404758.1:p.Ser60LysfsTer5
ENST00000424454.5:c.*321dup	ENSP00000404125.2:n.*321dup
ENST00000428935.5:c.186dup	ENSP00000399706.2:p.Val63SerfsTer?
ENST00000439676.5:c.178dup	ENSP00000415727.1:p.Ser60LysfsTer5
ENST00000442148.5:c.178dup	ENSP00000400848.1:p.Ser60LysfsTer5
ENST00000628285.2:c.186dup	ENSP00000486994.1:p.Val63SerfsTer?
NM_016628.4:c.313dup	NP_057712.2:p.Ser105LysfsTer5
NM_100264.2:c.178dup	NP_567822.1:p.Ser60LysfsTer5
NM_100486.3:c.313dup	NP_567823.1:p.Ser105LysfsTer5
XM_005252454.2:c.331dup	XP_005252511.1:p.Ser111LysfsTer5
XM_011519491.1:c.178dup	XP_011517793.1:p.Ser60LysfsTer5
XR_930491.1:n.233dup
XM_017016315.2:c.178dup	XP_016871804.1:p.Ser60LysfsTer5
XM_017016317.2:c.178dup	XP_016871806.1:p.Ser60LysfsTer5
XM_017016318.2:c.178dup	XP_016871807.1:p.Ser60LysfsTer5
XM_024448036.1:c.178dup	XP_024303804.1:p.Ser60LysfsTer5
XR_001747110.1:n.268dup
XR_930491.2:n.233dup
NM_016628.5:c.313dup MANE Select	NP_057712.2:p.Ser105LysfsTer5
NM_100264.3:c.178dup	NP_567822.1:p.Ser60LysfsTer5
NM_100486.4:c.313dup	NP_567823.1:p.Ser105LysfsTer5