Canonical Allele Identifier: CA358845935

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210625A>T (hg19) ; chr4:g.183289472A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289472A>T , CM000666.2:g.183289472A>T	GRCh38
NC_000004.11:g.184210625A>T , CM000666.1:g.184210625A>T	GRCh37
NC_000004.10:g.184447619A>T	NCBI36
NG_051586.1:g.195838A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3221A>T MANE Select	ENSP00000384222.3:p.Gln1074Leu
ENST00000403733.7:c.3221A>T	ENSP00000384222.3:p.Gln1074Leu
ENST00000427431.5:c.*2613A>T	ENSP00000393342.1:n.*2613A>T
ENST00000438543.5:c.*1017A>T	ENSP00000413521.1:n.*1017A>T
ENST00000448232.6:c.3293A>T	ENSP00000398577.2:p.Gln1098Leu
ENST00000504005.5:c.2267A>T	ENSP00000427569.1:p.Gln756Leu
ENST00000508747.1:c.605A>T	ENSP00000420835.1:p.Gln202Leu
ENST00000513834.5:c.3074A>T	ENSP00000425054.1:p.Gln1025Leu
NM_024949.5:c.3221A>T	NP_079225.5:p.Gln1074Leu
XM_011532269.1:c.3293A>T	XP_011530571.1:p.Gln1098Leu
XM_011532269.3:c.3293A>T	XP_011530571.1:p.Gln1098Leu
XM_024454225.1:c.2999A>T	XP_024309993.1:p.Gln1000Leu
NM_024949.6:c.3221A>T MANE Select	NP_079225.5:p.Gln1074Leu