Canonical Allele Identifier: CA507317805

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593871C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102969C>A , CM000681.2:g.36102969C>A	GRCh38
NC_000019.9:g.36593871C>A , CM000681.1:g.36593871C>A	GRCh37
NC_000019.8:g.41285711C>A	NCBI36
NG_028101.1:g.53089C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3342C>A	ENSP00000270301.6:p.Pro1114=
ENST00000401500.7:c.3357C>A MANE Select	ENSP00000384792.1:p.Pro1119=
ENST00000587391.6:c.*3217C>A	ENSP00000465525.1:n.*3217C>A
ENST00000679357.1:c.1437C>A
ENST00000679598.1:c.122C>A
ENST00000679682.1:c.3342C>A	ENSP00000506226.1:p.Pro1114=
ENST00000679714.1:c.3351C>A	ENSP00000506627.1:p.Pro1117=
ENST00000679757.1:c.3006C>A	ENSP00000505158.1:p.Pro1002=
ENST00000679858.1:c.*2739C>A	ENSP00000505655.1:n.*2739C>A
ENST00000680211.1:c.-43C>A	ENSP00000506102.1:n.-43C>A
ENST00000680280.1:n.644C>A
ENST00000680349.1:n.1925C>A
ENST00000680403.1:c.3342C>A	ENSP00000505677.1:p.Pro1114=
ENST00000680564.1:c.3108C>A	ENSP00000505582.1:p.Pro1036=
ENST00000680590.1:c.*1737C>A	ENSP00000505350.1:n.*1737C>A
ENST00000680597.1:c.122C>A
ENST00000680739.1:c.372C>A
ENST00000680773.1:n.1858C>A
ENST00000680806.1:c.*2660C>A	ENSP00000506418.1:n.*2660C>A
ENST00000680997.1:n.1289C>A
ENST00000681608.1:n.986C>A
ENST00000681625.1:c.*689C>A	ENSP00000505555.1:n.*689C>A
ENST00000681648.1:n.656C>A
ENST00000270301.11:c.3342C>A	ENSP00000270301.6:p.Pro1114=
ENST00000401500.6:c.3357C>A	ENSP00000384792.1:p.Pro1119=
ENST00000587391.5:c.*3217C>A	ENSP00000465525.1:n.*3217C>A
NM_001083961.1:c.3357C>A	NP_001077430.1:p.Pro1119=
NM_173636.4:c.3342C>A	NP_775907.4:p.Pro1114=
XM_005258809.2:c.3246C>A	XP_005258866.1:p.Pro1082=
XM_011526837.1:c.3342C>A	XP_011525139.1:p.Pro1114=
XM_011526838.1:c.3108C>A	XP_011525140.1:p.Pro1036=
XM_011526839.1:c.3006C>A	XP_011525141.1:p.Pro1002=
XM_011526840.1:c.2349C>A	XP_011525142.1:p.Pro783=
XM_011526841.1:c.1935C>A	XP_011525143.1:p.Pro645=
XM_011526842.1:c.1788C>A	XP_011525144.1:p.Pro596=
XM_011526843.1:c.1104C>A	XP_011525145.1:p.Pro368=
XM_011526844.1:c.1104C>A	XP_011525146.1:p.Pro368=
XM_011526840.2:c.2349C>A	XP_011525142.1:p.Pro783=
XM_011526841.2:c.1935C>A	XP_011525143.1:p.Pro645=
XM_011526844.2:c.1104C>A	XP_011525146.1:p.Pro368=
XM_017026665.1:c.3357C>A	XP_016882154.1:p.Pro1119=
NM_001083961.2:c.3357C>A MANE Select	NP_001077430.1:p.Pro1119=
NM_173636.5:c.3342C>A	NP_775907.4:p.Pro1114=