Canonical Allele Identifier: CA358845747

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210580A>C (hg19) ; chr4:g.183289427A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289427A>C , CM000666.2:g.183289427A>C	GRCh38
NC_000004.11:g.184210580A>C , CM000666.1:g.184210580A>C	GRCh37
NC_000004.10:g.184447574A>C	NCBI36
NG_051586.1:g.195793A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3176A>C MANE Select	ENSP00000384222.3:p.Gln1059Pro
ENST00000403733.7:c.3176A>C	ENSP00000384222.3:p.Gln1059Pro
ENST00000427431.5:c.*2568A>C	ENSP00000393342.1:n.*2568A>C
ENST00000438543.5:c.*972A>C	ENSP00000413521.1:n.*972A>C
ENST00000448232.6:c.3248A>C	ENSP00000398577.2:p.Gln1083Pro
ENST00000504005.5:c.2222A>C	ENSP00000427569.1:p.Gln741Pro
ENST00000508747.1:c.560A>C	ENSP00000420835.1:p.Gln187Pro
ENST00000513834.5:c.3029A>C	ENSP00000425054.1:p.Gln1010Pro
NM_024949.5:c.3176A>C	NP_079225.5:p.Gln1059Pro
XM_011532269.1:c.3248A>C	XP_011530571.1:p.Gln1083Pro
XM_011532269.3:c.3248A>C	XP_011530571.1:p.Gln1083Pro
XM_024454225.1:c.2954A>C	XP_024309993.1:p.Gln985Pro
NM_024949.6:c.3176A>C MANE Select	NP_079225.5:p.Gln1059Pro