Canonical Allele Identifier: CA507318554

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104564-C-G
• MyVariant Identifiers: chr19:g.36595466C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104564C>G , CM000681.2:g.36104564C>G	GRCh38
NC_000019.9:g.36595466C>G , CM000681.1:g.36595466C>G	GRCh37
NC_000019.8:g.41287306C>G	NCBI36
NG_028101.1:g.54684C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4185C>G	ENSP00000270301.6:p.Pro1395=
ENST00000401500.7:c.4200C>G MANE Select	ENSP00000384792.1:p.Pro1400=
ENST00000587391.6:c.*4060C>G	ENSP00000465525.1:n.*4060C>G
ENST00000679357.1:c.2280C>G
ENST00000679598.1:c.945C>G
ENST00000679682.1:c.4185C>G	ENSP00000506226.1:p.Pro1395=
ENST00000679714.1:c.4194C>G	ENSP00000506627.1:p.Pro1398=
ENST00000679757.1:c.3849C>G	ENSP00000505158.1:p.Pro1283=
ENST00000679858.1:c.*3582C>G	ENSP00000505655.1:n.*3582C>G
ENST00000680211.1:c.801C>G	ENSP00000506102.1:p.Pro267=
ENST00000680280.1:n.1703C>G
ENST00000680349.1:n.2849C>G
ENST00000680403.1:c.4185C>G	ENSP00000505677.1:p.Pro1395=
ENST00000680564.1:c.3951C>G	ENSP00000505582.1:p.Pro1317=
ENST00000680590.1:c.*2580C>G	ENSP00000505350.1:n.*2580C>G
ENST00000680597.1:c.933C>G
ENST00000680739.1:c.1215C>G
ENST00000680773.1:n.2701C>G
ENST00000680806.1:c.*3503C>G	ENSP00000506418.1:n.*3503C>G
ENST00000680997.1:n.2132C>G
ENST00000681608.1:n.2045C>G
ENST00000681625.1:c.*1532C>G	ENSP00000505555.1:n.*1532C>G
ENST00000681648.1:n.2251C>G
ENST00000270301.11:c.4185C>G	ENSP00000270301.6:p.Pro1395=
ENST00000401500.6:c.4200C>G	ENSP00000384792.1:p.Pro1400=
ENST00000587391.5:c.*4060C>G	ENSP00000465525.1:n.*4060C>G
NM_001083961.1:c.4200C>G	NP_001077430.1:p.Pro1400=
NM_173636.4:c.4185C>G	NP_775907.4:p.Pro1395=
XM_005258809.2:c.4089C>G	XP_005258866.1:p.Pro1363=
XM_011526837.1:c.4185C>G	XP_011525139.1:p.Pro1395=
XM_011526838.1:c.3951C>G	XP_011525140.1:p.Pro1317=
XM_011526839.1:c.3849C>G	XP_011525141.1:p.Pro1283=
XM_011526840.1:c.3192C>G	XP_011525142.1:p.Pro1064=
XM_011526841.1:c.2778C>G	XP_011525143.1:p.Pro926=
XM_011526842.1:c.2631C>G	XP_011525144.1:p.Pro877=
XM_011526843.1:c.1947C>G	XP_011525145.1:p.Pro649=
XM_011526844.1:c.1947C>G	XP_011525146.1:p.Pro649=
XM_011526840.2:c.3192C>G	XP_011525142.1:p.Pro1064=
XM_011526841.2:c.2778C>G	XP_011525143.1:p.Pro926=
XM_011526844.2:c.1947C>G	XP_011525146.1:p.Pro649=
XM_017026665.1:c.4200C>G	XP_016882154.1:p.Pro1400=
NM_001083961.2:c.4200C>G MANE Select	NP_001077430.1:p.Pro1400=
NM_173636.5:c.4185C>G	NP_775907.4:p.Pro1395=