Canonical Allele Identifier: CA507318628

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595493A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104591A>T , CM000681.2:g.36104591A>T	GRCh38
NC_000019.9:g.36595493A>T , CM000681.1:g.36595493A>T	GRCh37
NC_000019.8:g.41287333A>T	NCBI36
NG_028101.1:g.54711A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4212A>T	ENSP00000270301.6:p.Pro1404=
ENST00000401500.7:c.4227A>T MANE Select	ENSP00000384792.1:p.Pro1409=
ENST00000587391.6:c.*4087A>T	ENSP00000465525.1:n.*4087A>T
ENST00000679357.1:c.2307A>T
ENST00000679598.1:c.972A>T
ENST00000679682.1:c.4212A>T	ENSP00000506226.1:p.Pro1404=
ENST00000679714.1:c.4221A>T	ENSP00000506627.1:p.Pro1407=
ENST00000679757.1:c.3876A>T	ENSP00000505158.1:p.Pro1292=
ENST00000679858.1:c.*3609A>T	ENSP00000505655.1:n.*3609A>T
ENST00000680211.1:c.828A>T	ENSP00000506102.1:p.Pro276=
ENST00000680280.1:n.1730A>T
ENST00000680349.1:n.2876A>T
ENST00000680403.1:c.4212A>T	ENSP00000505677.1:p.Pro1404=
ENST00000680564.1:c.3978A>T	ENSP00000505582.1:p.Pro1326=
ENST00000680590.1:c.*2607A>T	ENSP00000505350.1:n.*2607A>T
ENST00000680597.1:c.960A>T
ENST00000680739.1:c.1242A>T
ENST00000680773.1:n.2728A>T
ENST00000680806.1:c.*3530A>T	ENSP00000506418.1:n.*3530A>T
ENST00000680997.1:n.2159A>T
ENST00000681608.1:n.2072A>T
ENST00000681625.1:c.*1559A>T	ENSP00000505555.1:n.*1559A>T
ENST00000681648.1:n.2278A>T
ENST00000270301.11:c.4212A>T	ENSP00000270301.6:p.Pro1404=
ENST00000401500.6:c.4227A>T	ENSP00000384792.1:p.Pro1409=
ENST00000587391.5:c.*4087A>T	ENSP00000465525.1:n.*4087A>T
NM_001083961.1:c.4227A>T	NP_001077430.1:p.Pro1409=
NM_173636.4:c.4212A>T	NP_775907.4:p.Pro1404=
XM_005258809.2:c.4116A>T	XP_005258866.1:p.Pro1372=
XM_011526837.1:c.4212A>T	XP_011525139.1:p.Pro1404=
XM_011526838.1:c.3978A>T	XP_011525140.1:p.Pro1326=
XM_011526839.1:c.3876A>T	XP_011525141.1:p.Pro1292=
XM_011526840.1:c.3219A>T	XP_011525142.1:p.Pro1073=
XM_011526841.1:c.2805A>T	XP_011525143.1:p.Pro935=
XM_011526842.1:c.2658A>T	XP_011525144.1:p.Pro886=
XM_011526843.1:c.1974A>T	XP_011525145.1:p.Pro658=
XM_011526844.1:c.1974A>T	XP_011525146.1:p.Pro658=
XM_011526840.2:c.3219A>T	XP_011525142.1:p.Pro1073=
XM_011526841.2:c.2805A>T	XP_011525143.1:p.Pro935=
XM_011526844.2:c.1974A>T	XP_011525146.1:p.Pro658=
XM_017026665.1:c.4227A>T	XP_016882154.1:p.Pro1409=
NM_001083961.2:c.4227A>T MANE Select	NP_001077430.1:p.Pro1409=
NM_173636.5:c.4212A>T	NP_775907.4:p.Pro1404=