Canonical Allele Identifier: CA1599433112

Gene: WWC1

Linked Data

• dbSNP Id: rs1582227808

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168418653T>C , CM000667.2:g.168418653T>C	GRCh38
NC_000005.9:g.167845658T>C , CM000667.1:g.167845658T>C	GRCh37
NC_000005.8:g.167778236T>C	NCBI36
NG_016712.1:g.131594T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265293.9:c.1185-3355T>C MANE Select	ENSP00000265293.4:n.1185-3355T>C
ENST00000265293.8:c.1185-3355T>C	ENSP00000265293.4:n.1185-3355T>C
ENST00000393895.7:c.1069-3355T>C
ENST00000517425.5:n.703-3355T>C
ENST00000518334.1:n.462-3355T>C
ENST00000521089.5:c.1185-3355T>C	ENSP00000427772.1:n.1185-3355T>C
ENST00000524228.5:c.514-3355T>C
NM_001161661.1:c.1185-3355T>C	NP_001155133.1:n.1185-3355T>C
NM_001161662.1:c.1185-3355T>C	NP_001155134.1:n.1185-3355T>C
NM_015238.2:c.1185-3355T>C	NP_056053.1:n.1185-3355T>C
XM_005265850.1:c.1185-3355T>C	XP_005265907.1:n.1185-3355T>C
XM_005265853.1:c.1185-3355T>C	XP_005265910.1:n.1185-3355T>C
XM_011534485.1:c.1368-3355T>C	XP_011532787.1:n.1368-3355T>C
XM_011534486.1:c.1368-3355T>C	XP_011532788.1:n.1368-3355T>C
XM_011534487.1:c.1368-3355T>C	XP_011532789.1:n.1368-3355T>C
XM_011534488.1:c.1368-3355T>C	XP_011532790.1:n.1368-3355T>C
XM_011534489.1:c.1368-3355T>C	XP_011532791.1:n.1368-3355T>C
XM_011534490.1:c.1368-3355T>C	XP_011532792.1:n.1368-3355T>C
XM_011534491.1:c.1368-3355T>C	XP_011532793.1:n.1368-3355T>C
XM_005265853.2:c.1185-3355T>C	XP_005265910.1:n.1185-3355T>C
XM_017009276.1:c.1368-3355T>C	XP_016864765.1:n.1368-3355T>C
XM_017009278.1:c.903-3355T>C	XP_016864767.1:n.903-3355T>C
NM_001161661.2:c.1185-3355T>C	NP_001155133.1:n.1185-3355T>C
NM_001161662.2:c.1185-3355T>C	NP_001155134.1:n.1185-3355T>C
NM_015238.3:c.1185-3355T>C MANE Select	NP_056053.1:n.1185-3355T>C