Canonical Allele Identifier: CA376404459

Gene: WAC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28614566G>T , CM000672.2:g.28614566G>T	GRCh38
NC_000010.10:g.28903495G>T , CM000672.1:g.28903495G>T	GRCh37
NC_000010.9:g.28943501G>T	NCBI36
NG_046603.1:g.86979G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495268.3:c.1530-1G>T	ENSP00000514964.1:n.1530-1G>T
ENST00000700325.1:c.1426-1G>T	ENSP00000514952.1:n.1426-1G>T
ENST00000706612.1:c.1426-1G>T	ENSP00000516469.1:n.1426-1G>T
ENST00000354911.9:c.1438-1G>T MANE Select	ENSP00000346986.4:n.1438-1G>T
ENST00000414108.6:c.1303-1G>T	ENSP00000415645.2:n.1303-1G>T
ENST00000420266.6:c.*1352-1G>T	ENSP00000404758.2:n.*1352-1G>T
ENST00000442148.6:c.1303-1G>T	ENSP00000400848.2:n.1303-1G>T
ENST00000628285.3:c.*864-1G>T	ENSP00000486994.2:n.*864-1G>T
ENST00000679398.1:c.1303-1G>T	ENSP00000506624.1:n.1303-1G>T
ENST00000679428.1:c.1303-1G>T	ENSP00000506445.1:n.1303-1G>T
ENST00000679570.1:c.*1433-1G>T	ENSP00000506705.1:n.*1433-1G>T
ENST00000680735.1:c.1309-1G>T	ENSP00000505513.1:n.1309-1G>T
ENST00000681112.1:c.*1291-1G>T	ENSP00000505444.1:n.*1291-1G>T
ENST00000345541.6:n.2179-1G>T
ENST00000347934.8:c.1129-1G>T	ENSP00000311106.4:n.1129-1G>T
ENST00000354911.8:c.1438-1G>T	ENSP00000346986.4:n.1438-1G>T
ENST00000375646.5:c.982-1G>T	ENSP00000364797.1:n.982-1G>T
ENST00000375664.8:c.1303-1G>T	ENSP00000364816.3:n.1303-1G>T
ENST00000439676.5:c.*219-1G>T	ENSP00000415727.1:n.*219-1G>T
ENST00000628285.2:c.*1091-1G>T	ENSP00000486994.1:n.*1091-1G>T
NM_016628.4:c.1438-1G>T	NP_057712.2:n.1438-1G>T
NM_100264.2:c.1303-1G>T	NP_567822.1:n.1303-1G>T
NM_100486.3:c.1129-1G>T	NP_567823.1:n.1129-1G>T
XM_005252454.2:c.1456-1G>T	XP_005252511.1:n.1456-1G>T
XM_011519491.1:c.1303-1G>T	XP_011517793.1:n.1303-1G>T
XR_930491.1:n.1585-1G>T
XM_017016315.2:c.1303-1G>T	XP_016871804.1:n.1303-1G>T
XM_017016317.2:c.994-1G>T	XP_016871806.1:n.994-1G>T
XM_017016318.2:c.994-1G>T	XP_016871807.1:n.994-1G>T
XM_024448036.1:c.1303-1G>T	XP_024303804.1:n.1303-1G>T
XR_001747110.1:n.1620-1G>T
XR_930491.2:n.1585-1G>T
NM_016628.5:c.1438-1G>T MANE Select	NP_057712.2:n.1438-1G>T
NM_100264.3:c.1303-1G>T	NP_567822.1:n.1303-1G>T
NM_100486.4:c.1129-1G>T	NP_567823.1:n.1129-1G>T