Canonical Allele Identifier: CA284091818

Gene: WDR59

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74944720G>A , CM000678.2:g.74944720G>A	GRCh38
NC_000016.9:g.74978618G>A , CM000678.1:g.74978618G>A	GRCh37
NC_000016.8:g.73536119G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262144.11:c.446-1894C>T MANE Select	ENSP00000262144.6:n.446-1894C>T
ENST00000262144.10:c.446-1894C>T	ENSP00000262144.6:n.446-1894C>T
ENST00000536050.5:c.383-1894C>T	ENSP00000481730.1:n.383-1894C>T
ENST00000563111.2:c.383-1894C>T	ENSP00000456139.1:n.383-1894C>T
ENST00000568323.5:n.542+3799C>T
ENST00000568462.5:n.379+3799C>T
ENST00000616369.4:c.446-1894C>T	ENSP00000482446.1:n.446-1894C>T
NM_030581.3:c.446-1894C>T	NP_085058.3:n.446-1894C>T
XM_005256146.2:c.446-1894C>T	XP_005256203.1:n.446-1894C>T
XM_011523331.1:c.-396-1894C>T	XP_011521633.1:n.-396-1894C>T
XR_933430.1:n.552-1894C>T
NM_001324171.1:c.446-1894C>T	NP_001311100.1:n.446-1894C>T
NM_001324172.1:c.446-1894C>T	NP_001311101.1:n.446-1894C>T
XM_005256146.3:c.446-1894C>T	XP_005256203.1:n.446-1894C>T
XM_017023667.2:c.-328-1894C>T	XP_016879156.1:n.-328-1894C>T
XM_017023668.2:c.-223+3799C>T	XP_016879157.1:n.-223+3799C>T
XM_017023669.1:c.-396-1894C>T	XP_016879158.1:n.-396-1894C>T
XM_017023670.1:c.-463-1894C>T	XP_016879159.1:n.-463-1894C>T
XM_024450446.1:c.-396-1894C>T	XP_024306214.1:n.-396-1894C>T
XR_933430.2:n.552-1894C>T
NM_030581.4:c.446-1894C>T MANE Select	NP_085058.3:n.446-1894C>T
NM_001324171.2:c.446-1894C>T	NP_001311100.1:n.446-1894C>T
NM_001324172.2:c.446-1894C>T	NP_001311101.1:n.446-1894C>T