Canonical Allele Identifier: CA1599433127

Gene: WWC1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168418661_168418662delinsCT , CM000667.2:g.168418661_168418662delinsCT	GRCh38
NC_000005.9:g.167845666_167845667delinsCT , CM000667.1:g.167845666_167845667delinsCT	GRCh37
NC_000005.8:g.167778244_167778245delinsCT	NCBI36
NG_016712.1:g.131602_131603delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265293.9:c.1185-3347_1185-3346delinsCT MANE Select	ENSP00000265293.4:n.1185-3347_1185-3346delinsCT
ENST00000265293.8:c.1185-3347_1185-3346delinsCT	ENSP00000265293.4:n.1185-3347_1185-3346delinsCT
ENST00000393895.7:c.1069-3347_1069-3346delinsCT
ENST00000517425.5:n.703-3347_703-3346delinsCT
ENST00000518334.1:n.462-3347_462-3346delinsCT
ENST00000521089.5:c.1185-3347_1185-3346delinsCT	ENSP00000427772.1:n.1185-3347_1185-3346delinsCT
ENST00000524228.5:c.514-3347_514-3346delinsCT
NM_001161661.1:c.1185-3347_1185-3346delinsCT	NP_001155133.1:n.1185-3347_1185-3346delinsCT
NM_001161662.1:c.1185-3347_1185-3346delinsCT	NP_001155134.1:n.1185-3347_1185-3346delinsCT
NM_015238.2:c.1185-3347_1185-3346delinsCT	NP_056053.1:n.1185-3347_1185-3346delinsCT
XM_005265850.1:c.1185-3347_1185-3346delinsCT	XP_005265907.1:n.1185-3347_1185-3346delinsCT
XM_005265853.1:c.1185-3347_1185-3346delinsCT	XP_005265910.1:n.1185-3347_1185-3346delinsCT
XM_011534485.1:c.1368-3347_1368-3346delinsCT	XP_011532787.1:n.1368-3347_1368-3346delinsCT
XM_011534486.1:c.1368-3347_1368-3346delinsCT	XP_011532788.1:n.1368-3347_1368-3346delinsCT
XM_011534487.1:c.1368-3347_1368-3346delinsCT	XP_011532789.1:n.1368-3347_1368-3346delinsCT
XM_011534488.1:c.1368-3347_1368-3346delinsCT	XP_011532790.1:n.1368-3347_1368-3346delinsCT
XM_011534489.1:c.1368-3347_1368-3346delinsCT	XP_011532791.1:n.1368-3347_1368-3346delinsCT
XM_011534490.1:c.1368-3347_1368-3346delinsCT	XP_011532792.1:n.1368-3347_1368-3346delinsCT
XM_011534491.1:c.1368-3347_1368-3346delinsCT	XP_011532793.1:n.1368-3347_1368-3346delinsCT
XM_005265853.2:c.1185-3347_1185-3346delinsCT	XP_005265910.1:n.1185-3347_1185-3346delinsCT
XM_017009276.1:c.1368-3347_1368-3346delinsCT	XP_016864765.1:n.1368-3347_1368-3346delinsCT
XM_017009278.1:c.903-3347_903-3346delinsCT	XP_016864767.1:n.903-3347_903-3346delinsCT
NM_001161661.2:c.1185-3347_1185-3346delinsCT	NP_001155133.1:n.1185-3347_1185-3346delinsCT
NM_001161662.2:c.1185-3347_1185-3346delinsCT	NP_001155134.1:n.1185-3347_1185-3346delinsCT
NM_015238.3:c.1185-3347_1185-3346delinsCT MANE Select	NP_056053.1:n.1185-3347_1185-3346delinsCT