Canonical Allele Identifier: CA792054658

Gene: WWC2

Linked Data

• dbSNP Id: rs1403372204
• gnomAD v3: 4-183289301-GCACCATCCAT-G
• gnomAD v4: 4-183289301-GCACCATCCAT-G
• MyVariant Identifiers: chr4:g.184210455_184210464del (hg19) ; chr4:g.183289302_183289311del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289304_183289313del , CM000666.2:g.183289304_183289313del	GRCh38
NC_000004.11:g.184210457_184210466del , CM000666.1:g.184210457_184210466del	GRCh37
NC_000004.10:g.184447451_184447460del	NCBI36
NG_051586.1:g.195670_195679del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3142-89_3142-80del MANE Select	ENSP00000384222.3:n.3142-89_3142-80del
ENST00000403733.7:c.3142-89_3142-80del	ENSP00000384222.3:n.3142-89_3142-80del
ENST00000427431.5:c.*2534-89_*2534-80del	ENSP00000393342.1:n.*2534-89_*2534-80del
ENST00000438543.5:c.*938-89_*938-80del	ENSP00000413521.1:n.*938-89_*938-80del
ENST00000448232.6:c.3214-89_3214-80del	ENSP00000398577.2:n.3214-89_3214-80del
ENST00000504005.5:c.2188-89_2188-80del	ENSP00000427569.1:n.2188-89_2188-80del
ENST00000508747.1:c.526-89_526-80del	ENSP00000420835.1:n.526-89_526-80del
ENST00000513834.5:c.2995-89_2995-80del	ENSP00000425054.1:n.2995-89_2995-80del
NM_024949.5:c.3142-89_3142-80del	NP_079225.5:n.3142-89_3142-80del
XM_011532269.1:c.3214-89_3214-80del	XP_011530571.1:n.3214-89_3214-80del
XM_011532269.3:c.3214-89_3214-80del	XP_011530571.1:n.3214-89_3214-80del
XM_024454225.1:c.2920-89_2920-80del	XP_024309993.1:n.2920-89_2920-80del
NM_024949.6:c.3142-89_3142-80del MANE Select	NP_079225.5:n.3142-89_3142-80del