Canonical Allele Identifier: CA204595257

Gene: WAC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28608384C>T , CM000672.2:g.28608384C>T	GRCh38
NC_000010.10:g.28897313C>T , CM000672.1:g.28897313C>T	GRCh37
NC_000010.9:g.28937319C>T	NCBI36
NG_046603.1:g.80797C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495268.3:c.446C>T	ENSP00000514964.1:p.Thr149Met
ENST00000700325.1:c.1106C>T	ENSP00000514952.1:p.Thr369Met
ENST00000706612.1:c.1106C>T	ENSP00000516469.1:p.Thr369Met
ENST00000354911.9:c.1118C>T MANE Select	ENSP00000346986.4:p.Thr373Met
ENST00000414108.6:c.983C>T	ENSP00000415645.2:p.Thr328Met
ENST00000420266.6:c.*1032C>T	ENSP00000404758.2:n.*1032C>T
ENST00000428935.6:c.*127C>T	ENSP00000399706.3:n.*127C>T
ENST00000442148.6:c.983C>T	ENSP00000400848.2:p.Thr328Met
ENST00000628285.3:c.*544C>T	ENSP00000486994.2:n.*544C>T
ENST00000679398.1:c.983C>T	ENSP00000506624.1:p.Thr328Met
ENST00000679428.1:c.983C>T	ENSP00000506445.1:p.Thr328Met
ENST00000679570.1:c.*1113C>T	ENSP00000506705.1:n.*1113C>T
ENST00000680735.1:c.989C>T	ENSP00000505513.1:p.Thr330Met
ENST00000681112.1:c.*971C>T	ENSP00000505444.1:n.*971C>T
ENST00000345541.6:n.916C>T
ENST00000347934.8:c.809C>T	ENSP00000311106.4:p.Thr270Met
ENST00000354911.8:c.1118C>T	ENSP00000346986.4:p.Thr373Met
ENST00000375646.5:c.674C>T	ENSP00000364797.1:p.Thr225Met
ENST00000375664.8:c.983C>T	ENSP00000364816.3:p.Thr328Met
ENST00000424454.5:c.*1126C>T	ENSP00000404125.2:n.*1126C>T
ENST00000428935.5:c.*544C>T	ENSP00000399706.2:n.*544C>T
ENST00000439676.5:c.983C>T	ENSP00000415727.1:p.Thr328Met
ENST00000476046.1:n.314C>T
ENST00000495268.2:n.39C>T
ENST00000628285.2:c.*544C>T	ENSP00000486994.1:n.*544C>T
NM_016628.4:c.1118C>T	NP_057712.2:p.Thr373Met
NM_100264.2:c.983C>T	NP_567822.1:p.Thr328Met
NM_100486.3:c.809C>T	NP_567823.1:p.Thr270Met
XM_005252454.2:c.1136C>T	XP_005252511.1:p.Thr379Met
XM_011519491.1:c.983C>T	XP_011517793.1:p.Thr328Met
XR_930491.1:n.1038C>T
XM_017016315.2:c.983C>T	XP_016871804.1:p.Thr328Met
XM_017016317.2:c.674C>T	XP_016871806.1:p.Thr225Met
XM_017016318.2:c.674C>T	XP_016871807.1:p.Thr225Met
XM_024448036.1:c.983C>T	XP_024303804.1:p.Thr328Met
XR_001747110.1:n.1073C>T
XR_930491.2:n.1038C>T
NM_016628.5:c.1118C>T MANE Select	NP_057712.2:p.Thr373Met
NM_100264.3:c.983C>T	NP_567822.1:p.Thr328Met
NM_100486.4:c.809C>T	NP_567823.1:p.Thr270Met