Canonical Allele Identifier: CA2608662016
Gene: WAC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.28595685C>A , CM000672.2:g.28595685C>A GRCh38
NC_000010.10:g.28884614C>A , CM000672.1:g.28884614C>A GRCh37
NC_000010.9:g.28924620C>A NCBI36
NG_046603.1:g.68098C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000700325.1:c.599-48C>A ENSP00000514952.1:n.599-48C>A
ENST00000706612.1:c.599-48C>A ENSP00000516469.1:n.599-48C>A
ENST00000354911.9:c.611-48C>A MANE Select ENSP00000346986.4:n.611-48C>A
ENST00000414108.6:c.476-48C>A ENSP00000415645.2:n.476-48C>A
ENST00000420266.6:c.*525-48C>A ENSP00000404758.2:n.*525-48C>A
ENST00000428935.6:c.476-10C>A ENSP00000399706.3:n.476-10C>A
ENST00000442148.6:c.476-48C>A ENSP00000400848.2:n.476-48C>A
ENST00000628285.3:c.*37-48C>A ENSP00000486994.2:n.*37-48C>A
ENST00000679398.1:c.476-48C>A ENSP00000506624.1:n.476-48C>A
ENST00000679428.1:c.476-48C>A ENSP00000506445.1:n.476-48C>A
ENST00000679570.1:c.*606-48C>A ENSP00000506705.1:n.*606-48C>A
ENST00000680735.1:c.482-48C>A ENSP00000505513.1:n.482-48C>A
ENST00000681112.1:c.*464-48C>A ENSP00000505444.1:n.*464-48C>A
ENST00000345541.6:n.409-48C>A
ENST00000347934.8:c.610+4853C>A ENSP00000311106.4:n.610+4853C>A
ENST00000354911.8:c.611-48C>A ENSP00000346986.4:n.611-48C>A
ENST00000375646.5:c.475+4853C>A ENSP00000364797.1:n.475+4853C>A
ENST00000375664.8:c.476-48C>A ENSP00000364816.3:n.476-48C>A
ENST00000414108.5:c.476-48C>A ENSP00000415645.1:n.476-48C>A
ENST00000420266.5:c.476-48C>A ENSP00000404758.1:n.476-48C>A
ENST00000424454.5:c.*619-48C>A ENSP00000404125.2:n.*619-48C>A
ENST00000428935.5:c.*37-48C>A ENSP00000399706.2:n.*37-48C>A
ENST00000439676.5:c.476-48C>A ENSP00000415727.1:n.476-48C>A
ENST00000442148.5:c.476-48C>A ENSP00000400848.1:n.476-48C>A
ENST00000628285.2:c.*37-48C>A ENSP00000486994.1:n.*37-48C>A
NM_016628.4:c.611-48C>A NP_057712.2:n.611-48C>A
NM_100264.2:c.476-48C>A NP_567822.1:n.476-48C>A
NM_100486.3:c.610+4853C>A NP_567823.1:n.610+4853C>A
XM_005252454.2:c.629-48C>A XP_005252511.1:n.629-48C>A
XM_011519491.1:c.476-48C>A XP_011517793.1:n.476-48C>A
XR_930491.1:n.531-48C>A
XM_017016315.2:c.476-48C>A XP_016871804.1:n.476-48C>A
XM_017016317.2:c.475+4853C>A XP_016871806.1:n.475+4853C>A
XM_017016318.2:c.475+4853C>A XP_016871807.1:n.475+4853C>A
XM_024448036.1:c.476-48C>A XP_024303804.1:n.476-48C>A
XR_001747110.1:n.566-48C>A
XR_930491.2:n.531-48C>A
NM_016628.5:c.611-48C>A MANE Select NP_057712.2:n.611-48C>A
NM_100264.3:c.476-48C>A NP_567822.1:n.476-48C>A
NM_100486.4:c.610+4853C>A NP_567823.1:n.610+4853C>A