Canonical Allele Identifier: CA16042696

Gene: WAC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28608338C>T , CM000672.2:g.28608338C>T	GRCh38
NC_000010.10:g.28897267C>T , CM000672.1:g.28897267C>T	GRCh37
NC_000010.9:g.28937273C>T	NCBI36
NG_046603.1:g.80751C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016628.5:c.1072C>T MANE Select	NP_057712.2:p.Gln358Ter
ENST00000354911.9:c.1072C>T MANE Select	ENSP00000346986.4:p.Gln358Ter
NM_016628.4:c.1072C>T	NP_057712.2:p.Gln358Ter
NM_100264.2:c.937C>T	NP_567822.1:p.Gln313Ter
NM_100264.3:c.937C>T	NP_567822.1:p.Gln313Ter
NM_100486.3:c.763C>T	NP_567823.1:p.Gln255Ter
NM_100486.4:c.763C>T	NP_567823.1:p.Gln255Ter
ENST00000345541.6:n.870C>T
ENST00000347934.8:c.763C>T	ENSP00000311106.4:p.Gln255Ter
ENST00000354911.8:c.1072C>T	ENSP00000346986.4:p.Gln358Ter
ENST00000375646.5:c.628C>T	ENSP00000364797.1:p.Gln210Ter
ENST00000375664.8:c.937C>T	ENSP00000364816.3:p.Gln313Ter
ENST00000414108.6:c.937C>T	ENSP00000415645.2:p.Gln313Ter
ENST00000420266.6:c.*986C>T	ENSP00000404758.2:n.*986C>T
ENST00000424454.5:c.*1080C>T	ENSP00000404125.2:n.*1080C>T
ENST00000428935.5:c.*498C>T	ENSP00000399706.2:n.*498C>T
ENST00000428935.6:c.*81C>T	ENSP00000399706.3:n.*81C>T
ENST00000439676.5:c.937C>T	ENSP00000415727.1:p.Gln313Ter
ENST00000442148.6:c.937C>T	ENSP00000400848.2:p.Gln313Ter
ENST00000476046.1:n.268C>T
ENST00000495268.3:c.400C>T	ENSP00000514964.1:p.Gln134Ter
ENST00000628285.2:c.*498C>T	ENSP00000486994.1:n.*498C>T
ENST00000628285.3:c.*498C>T	ENSP00000486994.2:n.*498C>T
ENST00000679398.1:c.937C>T	ENSP00000506624.1:p.Gln313Ter
ENST00000679428.1:c.937C>T	ENSP00000506445.1:p.Gln313Ter
ENST00000679570.1:c.*1067C>T	ENSP00000506705.1:n.*1067C>T
ENST00000680735.1:c.943C>T	ENSP00000505513.1:p.Gln315Ter
ENST00000681112.1:c.*925C>T	ENSP00000505444.1:n.*925C>T
ENST00000700325.1:c.1060C>T	ENSP00000514952.1:p.Gln354Ter
ENST00000706612.1:c.1060C>T	ENSP00000516469.1:p.Gln354Ter
XM_005252454.2:c.1090C>T	XP_005252511.1:p.Gln364Ter
XM_011519491.1:c.937C>T	XP_011517793.1:p.Gln313Ter
XM_017016315.2:c.937C>T	XP_016871804.1:p.Gln313Ter
XM_017016317.2:c.628C>T	XP_016871806.1:p.Gln210Ter
XM_017016318.2:c.628C>T	XP_016871807.1:p.Gln210Ter
XM_024448036.1:c.937C>T	XP_024303804.1:p.Gln313Ter
XR_001747110.1:n.1027C>T
XR_930491.1:n.992C>T
XR_930491.2:n.992C>T