Canonical Allele Identifier: CA1599414206

Gene: WWC1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168459457T= , CM000667.2:g.168459457T=	GRCh38
NC_000005.9:g.167886462T= , CM000667.1:g.167886462T=	GRCh37
NC_000005.8:g.167819040T=	NCBI36
NG_016712.1:g.172398T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265293.9:c.2824-1193T= MANE Select	ENSP00000265293.4:n.2824-1193T=
ENST00000265293.8:c.2824-1193T=	ENSP00000265293.4:n.2824-1193T=
ENST00000393895.7:c.2708-1193T=
ENST00000521089.5:c.2824-1193T=	ENSP00000427772.1:n.2824-1193T=
ENST00000522140.1:n.640-1193T=
ENST00000524038.5:c.802-1193T=	ENSP00000428084.1:n.802-1193T=
ENST00000524228.5:c.2153-1193T=
ENST00000619752.1:c.640-1193T=	ENSP00000483898.1:n.640-1193T=
NM_001161661.1:c.2824-1193T=	NP_001155133.1:n.2824-1193T=
NM_001161662.1:c.2824-1193T=	NP_001155134.1:n.2824-1193T=
NM_015238.2:c.2824-1193T=	NP_056053.1:n.2824-1193T=
XM_005265850.1:c.2839-1193T=	XP_005265907.1:n.2839-1193T=
XM_005265853.1:c.2824-1193T=	XP_005265910.1:n.2824-1193T=
XM_011534485.1:c.3022-1193T=	XP_011532787.1:n.3022-1193T=
XM_011534486.1:c.3022-1193T=	XP_011532788.1:n.3022-1193T=
XM_011534487.1:c.3007-1193T=	XP_011532789.1:n.3007-1193T=
XM_011534488.1:c.3022-1193T=	XP_011532790.1:n.3022-1193T=
XM_011534489.1:c.3007-1193T=	XP_011532791.1:n.3007-1193T=
XM_011534490.1:c.3022-1193T=	XP_011532792.1:n.3022-1193T=
XM_011534491.1:c.3007-1193T=	XP_011532793.1:n.3007-1193T=
XM_005265853.2:c.2824-1193T=	XP_005265910.1:n.2824-1193T=
XM_017009276.1:c.3007-1193T=	XP_016864765.1:n.3007-1193T=
XM_017009278.1:c.2557-1193T=	XP_016864767.1:n.2557-1193T=
NM_001161661.2:c.2824-1193T=	NP_001155133.1:n.2824-1193T=
NM_001161662.2:c.2824-1193T=	NP_001155134.1:n.2824-1193T=
NM_015238.3:c.2824-1193T= MANE Select	NP_056053.1:n.2824-1193T=