Canonical Allele Identifier: CA1599415907

Gene: WWC1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168461626G>C , CM000667.2:g.168461626G>C	GRCh38
NC_000005.9:g.167888631G>C , CM000667.1:g.167888631G>C	GRCh37
NC_000005.8:g.167821209G>C	NCBI36
NG_016712.1:g.174567G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265293.9:c.2916+884G>C MANE Select	ENSP00000265293.4:n.2916+884G>C
ENST00000265293.8:c.2916+884G>C	ENSP00000265293.4:n.2916+884G>C
ENST00000393895.7:c.2800+884G>C
ENST00000521089.5:c.2916+884G>C	ENSP00000427772.1:n.2916+884G>C
ENST00000522140.1:n.732+884G>C
ENST00000524038.5:c.894+884G>C	ENSP00000428084.1:n.894+884G>C
ENST00000524228.5:c.2245+884G>C
ENST00000619752.1:c.732+884G>C	ENSP00000483898.1:n.732+884G>C
NM_001161661.1:c.2916+884G>C	NP_001155133.1:n.2916+884G>C
NM_001161662.1:c.2916+884G>C	NP_001155134.1:n.2916+884G>C
NM_015238.2:c.2916+884G>C	NP_056053.1:n.2916+884G>C
XM_005265850.1:c.2931+884G>C	XP_005265907.1:n.2931+884G>C
XM_005265853.1:c.2916+884G>C	XP_005265910.1:n.2916+884G>C
XM_011534485.1:c.3114+884G>C	XP_011532787.1:n.3114+884G>C
XM_011534486.1:c.3114+884G>C	XP_011532788.1:n.3114+884G>C
XM_011534487.1:c.3099+884G>C	XP_011532789.1:n.3099+884G>C
XM_011534488.1:c.3114+884G>C	XP_011532790.1:n.3114+884G>C
XM_011534489.1:c.3099+884G>C	XP_011532791.1:n.3099+884G>C
XM_011534490.1:c.3114+884G>C	XP_011532792.1:n.3114+884G>C
XM_011534491.1:c.3099+884G>C	XP_011532793.1:n.3099+884G>C
XM_005265853.2:c.2916+884G>C	XP_005265910.1:n.2916+884G>C
XM_017009276.1:c.3099+884G>C	XP_016864765.1:n.3099+884G>C
XM_017009278.1:c.2649+884G>C	XP_016864767.1:n.2649+884G>C
NM_001161661.2:c.2916+884G>C	NP_001155133.1:n.2916+884G>C
NM_001161662.2:c.2916+884G>C	NP_001155134.1:n.2916+884G>C
NM_015238.3:c.2916+884G>C MANE Select	NP_056053.1:n.2916+884G>C