Canonical Allele Identifier: CA807273656
Gene: WWC1 HGNC NCBI

Linked Data

dbSNP Id: rs1344595362

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.168418658_168418660del , CM000667.2:g.168418658_168418660del GRCh38
NC_000005.9:g.167845663_167845665del , CM000667.1:g.167845663_167845665del GRCh37
NC_000005.8:g.167778241_167778243del NCBI36
NG_016712.1:g.131599_131601del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265293.9:c.1185-3350_1185-3348del MANE Select ENSP00000265293.4:n.1185-3350_1185-3348del
ENST00000265293.8:c.1185-3350_1185-3348del ENSP00000265293.4:n.1185-3350_1185-3348del
ENST00000393895.7:c.1069-3350_1069-3348del
ENST00000517425.5:n.703-3350_703-3348del
ENST00000518334.1:n.462-3350_462-3348del
ENST00000521089.5:c.1185-3350_1185-3348del ENSP00000427772.1:n.1185-3350_1185-3348del
ENST00000524228.5:c.514-3350_514-3348del
NM_001161661.1:c.1185-3350_1185-3348del NP_001155133.1:n.1185-3350_1185-3348del
NM_001161662.1:c.1185-3350_1185-3348del NP_001155134.1:n.1185-3350_1185-3348del
NM_015238.2:c.1185-3350_1185-3348del NP_056053.1:n.1185-3350_1185-3348del
XM_005265850.1:c.1185-3350_1185-3348del XP_005265907.1:n.1185-3350_1185-3348del
XM_005265853.1:c.1185-3350_1185-3348del XP_005265910.1:n.1185-3350_1185-3348del
XM_011534485.1:c.1368-3350_1368-3348del XP_011532787.1:n.1368-3350_1368-3348del
XM_011534486.1:c.1368-3350_1368-3348del XP_011532788.1:n.1368-3350_1368-3348del
XM_011534487.1:c.1368-3350_1368-3348del XP_011532789.1:n.1368-3350_1368-3348del
XM_011534488.1:c.1368-3350_1368-3348del XP_011532790.1:n.1368-3350_1368-3348del
XM_011534489.1:c.1368-3350_1368-3348del XP_011532791.1:n.1368-3350_1368-3348del
XM_011534490.1:c.1368-3350_1368-3348del XP_011532792.1:n.1368-3350_1368-3348del
XM_011534491.1:c.1368-3350_1368-3348del XP_011532793.1:n.1368-3350_1368-3348del
XM_005265853.2:c.1185-3350_1185-3348del XP_005265910.1:n.1185-3350_1185-3348del
XM_017009276.1:c.1368-3350_1368-3348del XP_016864765.1:n.1368-3350_1368-3348del
XM_017009278.1:c.903-3350_903-3348del XP_016864767.1:n.903-3350_903-3348del
NM_001161661.2:c.1185-3350_1185-3348del NP_001155133.1:n.1185-3350_1185-3348del
NM_001161662.2:c.1185-3350_1185-3348del NP_001155134.1:n.1185-3350_1185-3348del
NM_015238.3:c.1185-3350_1185-3348del MANE Select NP_056053.1:n.1185-3350_1185-3348del