Canonical Allele Identifier: CA1599421604

Gene: WWC1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168467849C= , CM000667.2:g.168467849C=	GRCh38
NC_000005.9:g.167894854C= , CM000667.1:g.167894854C=	GRCh37
NC_000005.8:g.167827432C=	NCBI36
NG_016712.1:g.180790C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265293.9:c.3160C= MANE Select	ENSP00000265293.4:p.Arg1054=
ENST00000265293.8:c.3160C=	ENSP00000265293.4:p.Arg1054=
ENST00000393895.7:c.3059C=
ENST00000518204.1:n.157C=
ENST00000521089.5:c.3178C=	ENSP00000427772.1:p.Arg1060=
ENST00000521391.1:n.42C=
ENST00000522140.1:n.976C=
ENST00000524038.5:c.1153C=	ENSP00000428084.1:p.Arg385=
ENST00000524228.5:c.2486C=
ENST00000619752.1:c.976C=	ENSP00000483898.1:p.Arg326=
NM_001161661.1:c.3178C=	NP_001155133.1:p.Arg1060=
NM_001161662.1:c.3175C=	NP_001155134.1:p.Arg1059=
NM_015238.2:c.3160C=	NP_056053.1:p.Arg1054=
XM_005265850.1:c.3193C=	XP_005265907.1:p.Arg1065=
XM_005265853.1:c.3157C=	XP_005265910.1:p.Arg1053=
XM_011534485.1:c.3376C=	XP_011532787.1:p.Arg1126=
XM_011534486.1:c.3373C=	XP_011532788.1:p.Arg1125=
XM_011534487.1:c.3361C=	XP_011532789.1:p.Arg1121=
XM_011534488.1:c.3358C=	XP_011532790.1:p.Arg1120=
XM_011534489.1:c.3358C=	XP_011532791.1:p.Arg1120=
XM_011534490.1:c.3355C=	XP_011532792.1:p.Arg1119=
XM_011534491.1:c.3343C=	XP_011532793.1:p.Arg1115=
XM_005265853.2:c.3157C=	XP_005265910.1:p.Arg1053=
XM_017009276.1:c.3340C=	XP_016864765.1:p.Arg1114=
XM_017009278.1:c.2911C=	XP_016864767.1:p.Arg971=
NM_001161661.2:c.3178C=	NP_001155133.1:p.Arg1060=
NM_001161662.2:c.3175C=	NP_001155134.1:p.Arg1059=
NM_015238.3:c.3160C= MANE Select	NP_056053.1:p.Arg1054=