Canonical Allele Identifier: CA2676371491

Gene: WWC1

Linked Data

• gnomAD v4: 5-168408396-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168408396G>T , CM000667.2:g.168408396G>T	GRCh38
NC_000005.9:g.167835401G>T , CM000667.1:g.167835401G>T	GRCh37
NC_000005.8:g.167767979G>T	NCBI36
NG_016712.1:g.121337G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265293.9:c.721-111G>T MANE Select	ENSP00000265293.4:n.721-111G>T
ENST00000265293.8:c.721-111G>T	ENSP00000265293.4:n.721-111G>T
ENST00000393895.7:c.605-111G>T
ENST00000517425.5:n.56-111G>T
ENST00000519659.5:n.71-111G>T
ENST00000521089.5:c.721-111G>T	ENSP00000427772.1:n.721-111G>T
ENST00000523043.5:n.498-111G>T
ENST00000524228.5:c.50-111G>T
NM_001161661.1:c.721-111G>T	NP_001155133.1:n.721-111G>T
NM_001161662.1:c.721-111G>T	NP_001155134.1:n.721-111G>T
NM_015238.2:c.721-111G>T	NP_056053.1:n.721-111G>T
XM_005265850.1:c.721-111G>T	XP_005265907.1:n.721-111G>T
XM_005265853.1:c.721-111G>T	XP_005265910.1:n.721-111G>T
XM_011534485.1:c.721-111G>T	XP_011532787.1:n.721-111G>T
XM_011534486.1:c.721-111G>T	XP_011532788.1:n.721-111G>T
XM_011534487.1:c.721-111G>T	XP_011532789.1:n.721-111G>T
XM_011534488.1:c.721-111G>T	XP_011532790.1:n.721-111G>T
XM_011534489.1:c.721-111G>T	XP_011532791.1:n.721-111G>T
XM_011534490.1:c.721-111G>T	XP_011532792.1:n.721-111G>T
XM_011534491.1:c.721-111G>T	XP_011532793.1:n.721-111G>T
XM_005265853.2:c.721-111G>T	XP_005265910.1:n.721-111G>T
XM_017009276.1:c.721-111G>T	XP_016864765.1:n.721-111G>T
XM_017009278.1:c.439-111G>T	XP_016864767.1:n.439-111G>T
NM_001161661.2:c.721-111G>T	NP_001155133.1:n.721-111G>T
NM_001161662.2:c.721-111G>T	NP_001155134.1:n.721-111G>T
NM_015238.3:c.721-111G>T MANE Select	NP_056053.1:n.721-111G>T