Canonical Allele Identifier: CA1599436790

Gene: WWC1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168408534C= , CM000667.2:g.168408534C=	GRCh38
NC_000005.9:g.167835539C= , CM000667.1:g.167835539C=	GRCh37
NC_000005.8:g.167768117C=	NCBI36
NG_016712.1:g.121475C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015238.3:c.748C= MANE Select	NP_056053.1:p.Arg250=
ENST00000265293.9:c.748C= MANE Select	ENSP00000265293.4:p.Arg250=
NM_001161661.1:c.748C=	NP_001155133.1:p.Arg250=
NM_001161661.2:c.748C=	NP_001155133.1:p.Arg250=
NM_001161662.1:c.748C=	NP_001155134.1:p.Arg250=
NM_001161662.2:c.748C=	NP_001155134.1:p.Arg250=
NM_015238.2:c.748C=	NP_056053.1:p.Arg250=
ENST00000265293.8:c.748C=	ENSP00000265293.4:p.Arg250=
ENST00000393895.7:c.632C=
ENST00000517425.5:n.83C=
ENST00000519659.5:n.98C=
ENST00000521089.5:c.748C=	ENSP00000427772.1:p.Arg250=
ENST00000523043.5:n.525C=
ENST00000524228.5:c.77C=
XM_005265850.1:c.748C=	XP_005265907.1:p.Arg250=
XM_005265853.1:c.748C=	XP_005265910.1:p.Arg250=
XM_005265853.2:c.748C=	XP_005265910.1:p.Arg250=
XM_011534485.1:c.748C=	XP_011532787.1:p.Arg250=
XM_011534486.1:c.748C=	XP_011532788.1:p.Arg250=
XM_011534487.1:c.748C=	XP_011532789.1:p.Arg250=
XM_011534488.1:c.748C=	XP_011532790.1:p.Arg250=
XM_011534489.1:c.748C=	XP_011532791.1:p.Arg250=
XM_011534490.1:c.748C=	XP_011532792.1:p.Arg250=
XM_011534491.1:c.748C=	XP_011532793.1:p.Arg250=
XM_017009276.1:c.748C=	XP_016864765.1:p.Arg250=
XM_017009278.1:c.466C=	XP_016864767.1:p.Arg156=