Canonical Allele Identifier: CA5454663

Gene: WAC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28534198C>T , CM000672.2:g.28534198C>T	GRCh38
NC_000010.10:g.28823127C>T , CM000672.1:g.28823127C>T	GRCh37
NC_000010.9:g.28863133C>T	NCBI36
NG_046603.1:g.6611C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700325.1:c.-58+164C>T	ENSP00000514952.1:n.-58+164C>T
ENST00000706612.1:c.68+164C>T	ENSP00000516469.1:n.68+164C>T
ENST00000354911.9:c.78+164C>T MANE Select	ENSP00000346986.4:n.78+164C>T
ENST00000414108.6:c.-58+16C>T	ENSP00000415645.2:n.-58+16C>T
ENST00000420266.6:c.226+16C>T	ENSP00000404758.2:n.226+16C>T
ENST00000428935.6:c.-58+164C>T	ENSP00000399706.3:n.-58+164C>T
ENST00000442148.6:c.-58+164C>T	ENSP00000400848.2:n.-58+164C>T
ENST00000628285.3:c.-58+164C>T	ENSP00000486994.2:n.-58+164C>T
ENST00000651441.1:c.-76+164C>T	ENSP00000498450.1:n.-76+164C>T
ENST00000651598.1:c.-76+164C>T	ENSP00000498480.1:n.-76+164C>T
ENST00000651885.1:c.78+164C>T	ENSP00000498678.1:n.78+164C>T
ENST00000679398.1:c.-58+164C>T	ENSP00000506624.1:n.-58+164C>T
ENST00000679428.1:c.-58+16C>T	ENSP00000506445.1:n.-58+16C>T
ENST00000679570.1:c.-58+164C>T	ENSP00000506705.1:n.-58+164C>T
ENST00000680735.1:c.-50+164C>T	ENSP00000505513.1:n.-50+164C>T
ENST00000681112.1:c.-58+164C>T	ENSP00000505444.1:n.-58+164C>T
ENST00000347934.8:c.78+164C>T	ENSP00000311106.4:n.78+164C>T
ENST00000354911.8:c.78+164C>T	ENSP00000346986.4:n.78+164C>T
ENST00000375646.5:c.-58+164C>T	ENSP00000364797.1:n.-58+164C>T
ENST00000375664.8:c.-58+164C>T	ENSP00000364816.3:n.-58+164C>T
ENST00000414108.5:c.-58+16C>T	ENSP00000415645.1:n.-58+16C>T
ENST00000420266.5:c.-58+164C>T	ENSP00000404758.1:n.-58+164C>T
ENST00000424454.5:c.79-36C>T	ENSP00000404125.2:n.79-36C>T
ENST00000428935.5:c.-162-36C>T	ENSP00000399706.2:n.-162-36C>T
ENST00000442148.5:c.-58+164C>T	ENSP00000400848.1:n.-58+164C>T
ENST00000448193.5:c.-58+164C>T	ENSP00000395008.1:n.-58+164C>T
ENST00000526722.1:c.-58+16C>T	ENSP00000434903.1:n.-58+16C>T
ENST00000528491.5:n.269+164C>T
ENST00000530865.5:n.61+164C>T
ENST00000532233.5:n.266+164C>T
NM_016628.4:c.78+164C>T	NP_057712.2:n.78+164C>T
NM_100264.2:c.-58+164C>T	NP_567822.1:n.-58+164C>T
NM_100486.3:c.78+164C>T	NP_567823.1:n.78+164C>T
XM_005252454.2:c.78+164C>T	XP_005252511.1:n.78+164C>T
XM_011519491.1:c.-58+16C>T	XP_011517793.1:n.-58+16C>T
XM_017016315.2:c.-58+164C>T	XP_016871804.1:n.-58+164C>T
XM_017016317.2:c.-58+164C>T	XP_016871806.1:n.-58+164C>T
XM_017016318.2:c.-58+164C>T	XP_016871807.1:n.-58+164C>T
XM_024448036.1:c.-58+164C>T	XP_024303804.1:n.-58+164C>T
XR_001747110.1:n.33+164C>T
NM_016628.5:c.78+164C>T MANE Select	NP_057712.2:n.78+164C>T
NM_100264.3:c.-58+164C>T	NP_567822.1:n.-58+164C>T
NM_100486.4:c.78+164C>T	NP_567823.1:n.78+164C>T