Canonical Allele Identifier: CA1599433531
Gene: WWC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.168418802T= , CM000667.2:g.168418802T= GRCh38
NC_000005.9:g.167845807T= , CM000667.1:g.167845807T= GRCh37
NC_000005.8:g.167778385T= NCBI36
NG_016712.1:g.131743T=

Transcript Alleles

HGVS Amino-acid change
ENST00000265293.9:c.1185-3206T= MANE Select ENSP00000265293.4:n.1185-3206T=
ENST00000265293.8:c.1185-3206T= ENSP00000265293.4:n.1185-3206T=
ENST00000393895.7:c.1069-3206T=
ENST00000517425.5:n.703-3206T=
ENST00000518334.1:n.462-3206T=
ENST00000521089.5:c.1185-3206T= ENSP00000427772.1:n.1185-3206T=
ENST00000524228.5:c.514-3206T=
NM_001161661.1:c.1185-3206T= NP_001155133.1:n.1185-3206T=
NM_001161662.1:c.1185-3206T= NP_001155134.1:n.1185-3206T=
NM_015238.2:c.1185-3206T= NP_056053.1:n.1185-3206T=
XM_005265850.1:c.1185-3206T= XP_005265907.1:n.1185-3206T=
XM_005265853.1:c.1185-3206T= XP_005265910.1:n.1185-3206T=
XM_011534485.1:c.1368-3206T= XP_011532787.1:n.1368-3206T=
XM_011534486.1:c.1368-3206T= XP_011532788.1:n.1368-3206T=
XM_011534487.1:c.1368-3206T= XP_011532789.1:n.1368-3206T=
XM_011534488.1:c.1368-3206T= XP_011532790.1:n.1368-3206T=
XM_011534489.1:c.1368-3206T= XP_011532791.1:n.1368-3206T=
XM_011534490.1:c.1368-3206T= XP_011532792.1:n.1368-3206T=
XM_011534491.1:c.1368-3206T= XP_011532793.1:n.1368-3206T=
XM_005265853.2:c.1185-3206T= XP_005265910.1:n.1185-3206T=
XM_017009276.1:c.1368-3206T= XP_016864765.1:n.1368-3206T=
XM_017009278.1:c.903-3206T= XP_016864767.1:n.903-3206T=
NM_001161661.2:c.1185-3206T= NP_001155133.1:n.1185-3206T=
NM_001161662.2:c.1185-3206T= NP_001155134.1:n.1185-3206T=
NM_015238.3:c.1185-3206T= MANE Select NP_056053.1:n.1185-3206T=