Canonical Allele Identifier: CA358845792

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289436-C-T
• MyVariant Identifiers: chr4:g.184210589C>T (hg19) ; chr4:g.183289436C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289436C>T , CM000666.2:g.183289436C>T	GRCh38
NC_000004.11:g.184210589C>T , CM000666.1:g.184210589C>T	GRCh37
NC_000004.10:g.184447583C>T	NCBI36
NG_051586.1:g.195802C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3185C>T MANE Select	ENSP00000384222.3:p.Pro1062Leu
ENST00000403733.7:c.3185C>T	ENSP00000384222.3:p.Pro1062Leu
ENST00000427431.5:c.*2577C>T	ENSP00000393342.1:n.*2577C>T
ENST00000438543.5:c.*981C>T	ENSP00000413521.1:n.*981C>T
ENST00000448232.6:c.3257C>T	ENSP00000398577.2:p.Pro1086Leu
ENST00000504005.5:c.2231C>T	ENSP00000427569.1:p.Pro744Leu
ENST00000508747.1:c.569C>T	ENSP00000420835.1:p.Pro190Leu
ENST00000513834.5:c.3038C>T	ENSP00000425054.1:p.Pro1013Leu
NM_024949.5:c.3185C>T	NP_079225.5:p.Pro1062Leu
XM_011532269.1:c.3257C>T	XP_011530571.1:p.Pro1086Leu
XM_011532269.3:c.3257C>T	XP_011530571.1:p.Pro1086Leu
XM_024454225.1:c.2963C>T	XP_024309993.1:p.Pro988Leu
NM_024949.6:c.3185C>T MANE Select	NP_079225.5:p.Pro1062Leu