Canonical Allele Identifier: CA442557695

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210734A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289581A>G , CM000666.2:g.183289581A>G	GRCh38
NC_000004.11:g.184210734A>G , CM000666.1:g.184210734A>G	GRCh37
NC_000004.10:g.184447728A>G	NCBI36
NG_051586.1:g.195947A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3330A>G MANE Select	ENSP00000384222.3:p.Pro1110=
ENST00000403733.7:c.3330A>G	ENSP00000384222.3:p.Pro1110=
ENST00000427431.5:c.*2722A>G	ENSP00000393342.1:n.*2722A>G
ENST00000438543.5:c.*1126A>G	ENSP00000413521.1:n.*1126A>G
ENST00000448232.6:c.3402A>G	ENSP00000398577.2:p.Pro1134=
ENST00000504005.5:c.2376A>G	ENSP00000427569.1:p.Pro792=
ENST00000508747.1:c.714A>G	ENSP00000420835.1:p.Pro238=
ENST00000513834.5:c.3183A>G	ENSP00000425054.1:p.Pro1061=
NM_024949.5:c.3330A>G	NP_079225.5:p.Pro1110=
XM_011532269.1:c.3402A>G	XP_011530571.1:p.Pro1134=
XM_011532269.3:c.3402A>G	XP_011530571.1:p.Pro1134=
XM_024454225.1:c.3108A>G	XP_024309993.1:p.Pro1036=
NM_024949.6:c.3330A>G MANE Select	NP_079225.5:p.Pro1110=