Canonical Allele Identifier: CA358846425

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210783A>C (hg19) ; chr4:g.183289630A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289630A>C , CM000666.2:g.183289630A>C	GRCh38
NC_000004.11:g.184210783A>C , CM000666.1:g.184210783A>C	GRCh37
NC_000004.10:g.184447777A>C	NCBI36
NG_051586.1:g.195996A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3379A>C MANE Select	ENSP00000384222.3:p.Lys1127Gln
ENST00000403733.7:c.3379A>C	ENSP00000384222.3:p.Lys1127Gln
ENST00000427431.5:c.*2771A>C	ENSP00000393342.1:n.*2771A>C
ENST00000438543.5:c.*1175A>C	ENSP00000413521.1:n.*1175A>C
ENST00000448232.6:c.3451A>C	ENSP00000398577.2:p.Lys1151Gln
ENST00000504005.5:c.2425A>C	ENSP00000427569.1:p.Lys809Gln
ENST00000508747.1:c.763A>C	ENSP00000420835.1:p.Lys255Gln
ENST00000513834.5:c.3232A>C	ENSP00000425054.1:p.Lys1078Gln
NM_024949.5:c.3379A>C	NP_079225.5:p.Lys1127Gln
XM_011532269.1:c.3451A>C	XP_011530571.1:p.Lys1151Gln
XM_011532269.3:c.3451A>C	XP_011530571.1:p.Lys1151Gln
XM_024454225.1:c.3157A>C	XP_024309993.1:p.Lys1053Gln
NM_024949.6:c.3379A>C MANE Select	NP_079225.5:p.Lys1127Gln