Canonical Allele Identifier: CA405461104

Gene: WDR62

Linked Data

• dbSNP Id: rs1001365242
• MyVariant Identifiers: chr19:g.36595530C>A (hg19) ; chr19:g.36104628C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104628C>A , CM000681.2:g.36104628C>A	GRCh38
NC_000019.9:g.36595530C>A , CM000681.1:g.36595530C>A	GRCh37
NC_000019.8:g.41287370C>A	NCBI36
NG_028101.1:g.54748C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4249C>A	ENSP00000270301.6:p.His1417Asn
ENST00000401500.7:c.4264C>A MANE Select	ENSP00000384792.1:p.His1422Asn
ENST00000587391.6:c.*4124C>A	ENSP00000465525.1:n.*4124C>A
ENST00000679357.1:c.2344C>A
ENST00000679598.1:c.1009C>A
ENST00000679682.1:c.4249C>A	ENSP00000506226.1:p.His1417Asn
ENST00000679714.1:c.4258C>A	ENSP00000506627.1:p.His1420Asn
ENST00000679757.1:c.3913C>A	ENSP00000505158.1:p.His1305Asn
ENST00000679858.1:c.*3646C>A	ENSP00000505655.1:n.*3646C>A
ENST00000680211.1:c.865C>A	ENSP00000506102.1:p.His289Asn
ENST00000680280.1:n.1767C>A
ENST00000680349.1:n.2913C>A
ENST00000680403.1:c.4249C>A	ENSP00000505677.1:p.His1417Asn
ENST00000680564.1:c.4015C>A	ENSP00000505582.1:p.His1339Asn
ENST00000680590.1:c.*2644C>A	ENSP00000505350.1:n.*2644C>A
ENST00000680597.1:c.997C>A
ENST00000680739.1:c.1279C>A
ENST00000680773.1:n.2765C>A
ENST00000680806.1:c.*3567C>A	ENSP00000506418.1:n.*3567C>A
ENST00000680997.1:n.2196C>A
ENST00000681608.1:n.2109C>A
ENST00000681625.1:c.*1596C>A	ENSP00000505555.1:n.*1596C>A
ENST00000681648.1:n.2315C>A
ENST00000270301.11:c.4249C>A	ENSP00000270301.6:p.His1417Asn
ENST00000401500.6:c.4264C>A	ENSP00000384792.1:p.His1422Asn
ENST00000587391.5:c.*4124C>A	ENSP00000465525.1:n.*4124C>A
NM_001083961.1:c.4264C>A	NP_001077430.1:p.His1422Asn
NM_173636.4:c.4249C>A	NP_775907.4:p.His1417Asn
XM_005258809.2:c.4153C>A	XP_005258866.1:p.His1385Asn
XM_011526837.1:c.4249C>A	XP_011525139.1:p.His1417Asn
XM_011526838.1:c.4015C>A	XP_011525140.1:p.His1339Asn
XM_011526839.1:c.3913C>A	XP_011525141.1:p.His1305Asn
XM_011526840.1:c.3256C>A	XP_011525142.1:p.His1086Asn
XM_011526841.1:c.2842C>A	XP_011525143.1:p.His948Asn
XM_011526842.1:c.2695C>A	XP_011525144.1:p.His899Asn
XM_011526843.1:c.2011C>A	XP_011525145.1:p.His671Asn
XM_011526844.1:c.2011C>A	XP_011525146.1:p.His671Asn
XM_011526840.2:c.3256C>A	XP_011525142.1:p.His1086Asn
XM_011526841.2:c.2842C>A	XP_011525143.1:p.His948Asn
XM_011526844.2:c.2011C>A	XP_011525146.1:p.His671Asn
XM_017026665.1:c.4264C>A	XP_016882154.1:p.His1422Asn
NM_001083961.2:c.4264C>A MANE Select	NP_001077430.1:p.His1422Asn
NM_173636.5:c.4249C>A	NP_775907.4:p.His1417Asn