Canonical Allele Identifier: CA14250183

Gene: WWP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.69796425A>G , CM000678.2:g.69796425A>G	GRCh38
NC_000016.9:g.69830328A>G , CM000678.1:g.69830328A>G	GRCh37
NC_000016.8:g.68387829A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359154.7:c.71-2257A>G MANE Select	ENSP00000352069.2:n.71-2257A>G
ENST00000359154.6:c.71-2257A>G	ENSP00000352069.2:n.71-2257A>G
ENST00000561780.5:c.71-2257A>G	ENSP00000456451.1:n.71-2257A>G
ENST00000563659.5:c.71-2257A>G	ENSP00000455347.1:n.71-2257A>G
ENST00000569174.5:c.71-2257A>G	ENSP00000455311.1:n.71-2257A>G
ENST00000569620.5:c.71-2257A>G	ENSP00000456582.1:n.71-2257A>G
ENST00000569658.1:n.116-2257A>G
NM_001270454.1:c.71-2257A>G	NP_001257383.1:n.71-2257A>G
NM_001270455.1:c.71-2257A>G	NP_001257384.1:n.71-2257A>G
NM_007014.4:c.71-2257A>G	NP_008945.2:n.71-2257A>G
XM_011522823.1:c.71-2257A>G	XP_011521125.1:n.71-2257A>G
XM_011522824.1:c.71-2257A>G	XP_011521126.1:n.71-2257A>G
XM_011522825.1:c.71-2257A>G	XP_011521127.1:n.71-2257A>G
XM_011522823.2:c.71-2257A>G	XP_011521125.1:n.71-2257A>G
XM_017022879.1:c.71-2257A>G	XP_016878368.1:n.71-2257A>G
XM_017022880.1:c.71-2257A>G	XP_016878369.1:n.71-2257A>G
XM_017022881.1:c.71-2257A>G	XP_016878370.1:n.71-2257A>G
NM_001270454.2:c.71-2257A>G MANE Select	NP_001257383.1:n.71-2257A>G
NM_001270455.2:c.71-2257A>G	NP_001257384.1:n.71-2257A>G
NM_007014.5:c.71-2257A>G	NP_008945.2:n.71-2257A>G