Canonical Allele Identifier: CA507318615

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104588-C-T
• MyVariant Identifiers: chr19:g.36595490C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104588C>T , CM000681.2:g.36104588C>T	GRCh38
NC_000019.9:g.36595490C>T , CM000681.1:g.36595490C>T	GRCh37
NC_000019.8:g.41287330C>T	NCBI36
NG_028101.1:g.54708C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4209C>T	ENSP00000270301.6:p.Pro1403=
ENST00000401500.7:c.4224C>T MANE Select	ENSP00000384792.1:p.Pro1408=
ENST00000587391.6:c.*4084C>T	ENSP00000465525.1:n.*4084C>T
ENST00000679357.1:c.2304C>T
ENST00000679598.1:c.969C>T
ENST00000679682.1:c.4209C>T	ENSP00000506226.1:p.Pro1403=
ENST00000679714.1:c.4218C>T	ENSP00000506627.1:p.Pro1406=
ENST00000679757.1:c.3873C>T	ENSP00000505158.1:p.Pro1291=
ENST00000679858.1:c.*3606C>T	ENSP00000505655.1:n.*3606C>T
ENST00000680211.1:c.825C>T	ENSP00000506102.1:p.Pro275=
ENST00000680280.1:n.1727C>T
ENST00000680349.1:n.2873C>T
ENST00000680403.1:c.4209C>T	ENSP00000505677.1:p.Pro1403=
ENST00000680564.1:c.3975C>T	ENSP00000505582.1:p.Pro1325=
ENST00000680590.1:c.*2604C>T	ENSP00000505350.1:n.*2604C>T
ENST00000680597.1:c.957C>T
ENST00000680739.1:c.1239C>T
ENST00000680773.1:n.2725C>T
ENST00000680806.1:c.*3527C>T	ENSP00000506418.1:n.*3527C>T
ENST00000680997.1:n.2156C>T
ENST00000681608.1:n.2069C>T
ENST00000681625.1:c.*1556C>T	ENSP00000505555.1:n.*1556C>T
ENST00000681648.1:n.2275C>T
ENST00000270301.11:c.4209C>T	ENSP00000270301.6:p.Pro1403=
ENST00000401500.6:c.4224C>T	ENSP00000384792.1:p.Pro1408=
ENST00000587391.5:c.*4084C>T	ENSP00000465525.1:n.*4084C>T
NM_001083961.1:c.4224C>T	NP_001077430.1:p.Pro1408=
NM_173636.4:c.4209C>T	NP_775907.4:p.Pro1403=
XM_005258809.2:c.4113C>T	XP_005258866.1:p.Pro1371=
XM_011526837.1:c.4209C>T	XP_011525139.1:p.Pro1403=
XM_011526838.1:c.3975C>T	XP_011525140.1:p.Pro1325=
XM_011526839.1:c.3873C>T	XP_011525141.1:p.Pro1291=
XM_011526840.1:c.3216C>T	XP_011525142.1:p.Pro1072=
XM_011526841.1:c.2802C>T	XP_011525143.1:p.Pro934=
XM_011526842.1:c.2655C>T	XP_011525144.1:p.Pro885=
XM_011526843.1:c.1971C>T	XP_011525145.1:p.Pro657=
XM_011526844.1:c.1971C>T	XP_011525146.1:p.Pro657=
XM_011526840.2:c.3216C>T	XP_011525142.1:p.Pro1072=
XM_011526841.2:c.2802C>T	XP_011525143.1:p.Pro934=
XM_011526844.2:c.1971C>T	XP_011525146.1:p.Pro657=
XM_017026665.1:c.4224C>T	XP_016882154.1:p.Pro1408=
NM_001083961.2:c.4224C>T MANE Select	NP_001077430.1:p.Pro1408=
NM_173636.5:c.4209C>T	NP_775907.4:p.Pro1403=