Canonical Allele Identifier: CA362091406

Gene: WWC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265293.9:c.3160C>G MANE Select	ENSP00000265293.4:p.Arg1054Gly
ENST00000265293.8:c.3160C>G	ENSP00000265293.4:p.Arg1054Gly
ENST00000393895.7:c.3059C>G
ENST00000518204.1:n.157C>G
ENST00000521089.5:c.3178C>G	ENSP00000427772.1:p.Arg1060Gly
ENST00000521391.1:n.42C>G
ENST00000522140.1:n.976C>G
ENST00000524038.5:c.1153C>G	ENSP00000428084.1:p.Arg385Gly
ENST00000524228.5:c.2486C>G
ENST00000619752.1:c.976C>G	ENSP00000483898.1:p.Arg326Gly
NM_001161661.1:c.3178C>G	NP_001155133.1:p.Arg1060Gly
NM_001161662.1:c.3175C>G	NP_001155134.1:p.Arg1059Gly
NM_015238.2:c.3160C>G	NP_056053.1:p.Arg1054Gly
XM_005265850.1:c.3193C>G	XP_005265907.1:p.Arg1065Gly
XM_005265853.1:c.3157C>G	XP_005265910.1:p.Arg1053Gly
XM_011534485.1:c.3376C>G	XP_011532787.1:p.Arg1126Gly
XM_011534486.1:c.3373C>G	XP_011532788.1:p.Arg1125Gly
XM_011534487.1:c.3361C>G	XP_011532789.1:p.Arg1121Gly
XM_011534488.1:c.3358C>G	XP_011532790.1:p.Arg1120Gly
XM_011534489.1:c.3358C>G	XP_011532791.1:p.Arg1120Gly
XM_011534490.1:c.3355C>G	XP_011532792.1:p.Arg1119Gly
XM_011534491.1:c.3343C>G	XP_011532793.1:p.Arg1115Gly
XM_005265853.2:c.3157C>G	XP_005265910.1:p.Arg1053Gly
XM_017009276.1:c.3340C>G	XP_016864765.1:p.Arg1114Gly
XM_017009278.1:c.2911C>G	XP_016864767.1:p.Arg971Gly
NM_001161661.2:c.3178C>G	NP_001155133.1:p.Arg1060Gly
NM_001161662.2:c.3175C>G	NP_001155134.1:p.Arg1059Gly
NM_015238.3:c.3160C>G MANE Select	NP_056053.1:p.Arg1054Gly