Canonical Allele Identifier: CA926269073

Gene: WAC

Linked Data

• dbSNP Id: rs1840325666
• gnomAD v3: 10-28595681-TC-T
• gnomAD v4: 10-28595681-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28595682del , CM000672.2:g.28595682del	GRCh38
NC_000010.10:g.28884611del , CM000672.1:g.28884611del	GRCh37
NC_000010.9:g.28924617del	NCBI36
NG_046603.1:g.68095del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700325.1:c.599-51del	ENSP00000514952.1:n.599-51del
ENST00000706612.1:c.599-51del	ENSP00000516469.1:n.599-51del
ENST00000354911.9:c.611-51del MANE Select	ENSP00000346986.4:n.611-51del
ENST00000414108.6:c.476-51del	ENSP00000415645.2:n.476-51del
ENST00000420266.6:c.*525-51del	ENSP00000404758.2:n.*525-51del
ENST00000428935.6:c.476-13del	ENSP00000399706.3:n.476-13del
ENST00000442148.6:c.476-51del	ENSP00000400848.2:n.476-51del
ENST00000628285.3:c.*37-51del	ENSP00000486994.2:n.*37-51del
ENST00000679398.1:c.476-51del	ENSP00000506624.1:n.476-51del
ENST00000679428.1:c.476-51del	ENSP00000506445.1:n.476-51del
ENST00000679570.1:c.*606-51del	ENSP00000506705.1:n.*606-51del
ENST00000680735.1:c.482-51del	ENSP00000505513.1:n.482-51del
ENST00000681112.1:c.*464-51del	ENSP00000505444.1:n.*464-51del
ENST00000345541.6:n.409-51del
ENST00000347934.8:c.610+4850del	ENSP00000311106.4:n.610+4850del
ENST00000354911.8:c.611-51del	ENSP00000346986.4:n.611-51del
ENST00000375646.5:c.475+4850del	ENSP00000364797.1:n.475+4850del
ENST00000375664.8:c.476-51del	ENSP00000364816.3:n.476-51del
ENST00000414108.5:c.476-51del	ENSP00000415645.1:n.476-51del
ENST00000420266.5:c.476-51del	ENSP00000404758.1:n.476-51del
ENST00000424454.5:c.*619-51del	ENSP00000404125.2:n.*619-51del
ENST00000428935.5:c.*37-51del	ENSP00000399706.2:n.*37-51del
ENST00000439676.5:c.476-51del	ENSP00000415727.1:n.476-51del
ENST00000442148.5:c.476-51del	ENSP00000400848.1:n.476-51del
ENST00000628285.2:c.*37-51del	ENSP00000486994.1:n.*37-51del
NM_016628.4:c.611-51del	NP_057712.2:n.611-51del
NM_100264.2:c.476-51del	NP_567822.1:n.476-51del
NM_100486.3:c.610+4850del	NP_567823.1:n.610+4850del
XM_005252454.2:c.629-51del	XP_005252511.1:n.629-51del
XM_011519491.1:c.476-51del	XP_011517793.1:n.476-51del
XR_930491.1:n.531-51del
XM_017016315.2:c.476-51del	XP_016871804.1:n.476-51del
XM_017016317.2:c.475+4850del	XP_016871806.1:n.475+4850del
XM_017016318.2:c.475+4850del	XP_016871807.1:n.475+4850del
XM_024448036.1:c.476-51del	XP_024303804.1:n.476-51del
XR_001747110.1:n.566-51del
XR_930491.2:n.531-51del
NM_016628.5:c.611-51del MANE Select	NP_057712.2:n.611-51del
NM_100264.3:c.476-51del	NP_567822.1:n.476-51del
NM_100486.4:c.610+4850del	NP_567823.1:n.610+4850del