Canonical Allele Identifier: CA371438957

Gene: WWP1

Linked Data

• ClinVar Variation Id: 487621
• ClinVar RCV Id: RCV000656199
• dbSNP Id: rs773370868
• MyVariant Identifiers: chr8:g.87454888A>T (hg19) ; chr8:g.86442659A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86442659A>T , CM000670.2:g.86442659A>T	GRCh38
NC_000008.10:g.87454888A>T , CM000670.1:g.87454888A>T	GRCh37
NC_000008.9:g.87524004A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517970.6:c.1879A>T MANE Select	ENSP00000427793.1:p.Met627Leu
ENST00000265428.4:c.1879A>T	ENSP00000265428.4:p.Met627Leu
ENST00000517970.5:c.1879A>T	ENSP00000427793.1:p.Met627Leu
ENST00000518683.5:n.1533A>T
ENST00000520453.5:c.380A>T
ENST00000521997.5:n.224A>T
ENST00000524036.1:n.388A>T
NM_007013.3:c.1879A>T	NP_008944.1:p.Met627Leu
XM_005250760.2:c.1879A>T	XP_005250817.1:p.Met627Leu
XM_005250761.2:c.1876A>T	XP_005250818.1:p.Met626Leu
XM_011516802.1:c.1807A>T	XP_011515104.1:p.Met603Leu
XM_005250760.4:c.1879A>T	XP_005250817.1:p.Met627Leu
XM_005250761.4:c.1876A>T	XP_005250818.1:p.Met626Leu
XM_017012993.1:c.1876A>T	XP_016868482.1:p.Met626Leu
XM_017012994.2:c.1807A>T	XP_016868483.1:p.Met603Leu
XM_017012995.2:c.1342A>T	XP_016868484.1:p.Met448Leu
XM_017012996.1:c.1342A>T	XP_016868485.1:p.Met448Leu
XM_017012997.2:c.1270A>T	XP_016868486.1:p.Met424Leu
XM_024447056.1:c.1807A>T	XP_024302824.1:p.Met603Leu
XR_001745464.2:n.2157A>T
NM_007013.4:c.1879A>T MANE Select	NP_008944.1:p.Met627Leu