Canonical Allele Identifier: CA405460517

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595464C>G (hg19) ; chr19:g.36104562C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104562C>G , CM000681.2:g.36104562C>G	GRCh38
NC_000019.9:g.36595464C>G , CM000681.1:g.36595464C>G	GRCh37
NC_000019.8:g.41287304C>G	NCBI36
NG_028101.1:g.54682C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4183C>G	ENSP00000270301.6:p.Pro1395Ala
ENST00000401500.7:c.4198C>G MANE Select	ENSP00000384792.1:p.Pro1400Ala
ENST00000587391.6:c.*4058C>G	ENSP00000465525.1:n.*4058C>G
ENST00000679357.1:c.2278C>G
ENST00000679598.1:c.943C>G
ENST00000679682.1:c.4183C>G	ENSP00000506226.1:p.Pro1395Ala
ENST00000679714.1:c.4192C>G	ENSP00000506627.1:p.Pro1398Ala
ENST00000679757.1:c.3847C>G	ENSP00000505158.1:p.Pro1283Ala
ENST00000679858.1:c.*3580C>G	ENSP00000505655.1:n.*3580C>G
ENST00000680211.1:c.799C>G	ENSP00000506102.1:p.Pro267Ala
ENST00000680280.1:n.1701C>G
ENST00000680349.1:n.2847C>G
ENST00000680403.1:c.4183C>G	ENSP00000505677.1:p.Pro1395Ala
ENST00000680564.1:c.3949C>G	ENSP00000505582.1:p.Pro1317Ala
ENST00000680590.1:c.*2578C>G	ENSP00000505350.1:n.*2578C>G
ENST00000680597.1:c.931C>G
ENST00000680739.1:c.1213C>G
ENST00000680773.1:n.2699C>G
ENST00000680806.1:c.*3501C>G	ENSP00000506418.1:n.*3501C>G
ENST00000680997.1:n.2130C>G
ENST00000681608.1:n.2043C>G
ENST00000681625.1:c.*1530C>G	ENSP00000505555.1:n.*1530C>G
ENST00000681648.1:n.2249C>G
ENST00000270301.11:c.4183C>G	ENSP00000270301.6:p.Pro1395Ala
ENST00000401500.6:c.4198C>G	ENSP00000384792.1:p.Pro1400Ala
ENST00000587391.5:c.*4058C>G	ENSP00000465525.1:n.*4058C>G
NM_001083961.1:c.4198C>G	NP_001077430.1:p.Pro1400Ala
NM_173636.4:c.4183C>G	NP_775907.4:p.Pro1395Ala
XM_005258809.2:c.4087C>G	XP_005258866.1:p.Pro1363Ala
XM_011526837.1:c.4183C>G	XP_011525139.1:p.Pro1395Ala
XM_011526838.1:c.3949C>G	XP_011525140.1:p.Pro1317Ala
XM_011526839.1:c.3847C>G	XP_011525141.1:p.Pro1283Ala
XM_011526840.1:c.3190C>G	XP_011525142.1:p.Pro1064Ala
XM_011526841.1:c.2776C>G	XP_011525143.1:p.Pro926Ala
XM_011526842.1:c.2629C>G	XP_011525144.1:p.Pro877Ala
XM_011526843.1:c.1945C>G	XP_011525145.1:p.Pro649Ala
XM_011526844.1:c.1945C>G	XP_011525146.1:p.Pro649Ala
XM_011526840.2:c.3190C>G	XP_011525142.1:p.Pro1064Ala
XM_011526841.2:c.2776C>G	XP_011525143.1:p.Pro926Ala
XM_011526844.2:c.1945C>G	XP_011525146.1:p.Pro649Ala
XM_017026665.1:c.4198C>G	XP_016882154.1:p.Pro1400Ala
NM_001083961.2:c.4198C>G MANE Select	NP_001077430.1:p.Pro1400Ala
NM_173636.5:c.4183C>G	NP_775907.4:p.Pro1395Ala