Canonical Allele Identifier: CA507318714

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104621-C-T
• MyVariant Identifiers: chr19:g.36595523C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104621C>T , CM000681.2:g.36104621C>T	GRCh38
NC_000019.9:g.36595523C>T , CM000681.1:g.36595523C>T	GRCh37
NC_000019.8:g.41287363C>T	NCBI36
NG_028101.1:g.54741C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4242C>T	ENSP00000270301.6:p.Asn1414=
ENST00000401500.7:c.4257C>T MANE Select	ENSP00000384792.1:p.Asn1419=
ENST00000587391.6:c.*4117C>T	ENSP00000465525.1:n.*4117C>T
ENST00000679357.1:c.2337C>T
ENST00000679598.1:c.1002C>T
ENST00000679682.1:c.4242C>T	ENSP00000506226.1:p.Asn1414=
ENST00000679714.1:c.4251C>T	ENSP00000506627.1:p.Asn1417=
ENST00000679757.1:c.3906C>T	ENSP00000505158.1:p.Asn1302=
ENST00000679858.1:c.*3639C>T	ENSP00000505655.1:n.*3639C>T
ENST00000680211.1:c.858C>T	ENSP00000506102.1:p.Asn286=
ENST00000680280.1:n.1760C>T
ENST00000680349.1:n.2906C>T
ENST00000680403.1:c.4242C>T	ENSP00000505677.1:p.Asn1414=
ENST00000680564.1:c.4008C>T	ENSP00000505582.1:p.Asn1336=
ENST00000680590.1:c.*2637C>T	ENSP00000505350.1:n.*2637C>T
ENST00000680597.1:c.990C>T
ENST00000680739.1:c.1272C>T
ENST00000680773.1:n.2758C>T
ENST00000680806.1:c.*3560C>T	ENSP00000506418.1:n.*3560C>T
ENST00000680997.1:n.2189C>T
ENST00000681608.1:n.2102C>T
ENST00000681625.1:c.*1589C>T	ENSP00000505555.1:n.*1589C>T
ENST00000681648.1:n.2308C>T
ENST00000270301.11:c.4242C>T	ENSP00000270301.6:p.Asn1414=
ENST00000401500.6:c.4257C>T	ENSP00000384792.1:p.Asn1419=
ENST00000587391.5:c.*4117C>T	ENSP00000465525.1:n.*4117C>T
NM_001083961.1:c.4257C>T	NP_001077430.1:p.Asn1419=
NM_173636.4:c.4242C>T	NP_775907.4:p.Asn1414=
XM_005258809.2:c.4146C>T	XP_005258866.1:p.Asn1382=
XM_011526837.1:c.4242C>T	XP_011525139.1:p.Asn1414=
XM_011526838.1:c.4008C>T	XP_011525140.1:p.Asn1336=
XM_011526839.1:c.3906C>T	XP_011525141.1:p.Asn1302=
XM_011526840.1:c.3249C>T	XP_011525142.1:p.Asn1083=
XM_011526841.1:c.2835C>T	XP_011525143.1:p.Asn945=
XM_011526842.1:c.2688C>T	XP_011525144.1:p.Asn896=
XM_011526843.1:c.2004C>T	XP_011525145.1:p.Asn668=
XM_011526844.1:c.2004C>T	XP_011525146.1:p.Asn668=
XM_011526840.2:c.3249C>T	XP_011525142.1:p.Asn1083=
XM_011526841.2:c.2835C>T	XP_011525143.1:p.Asn945=
XM_011526844.2:c.2004C>T	XP_011525146.1:p.Asn668=
XM_017026665.1:c.4257C>T	XP_016882154.1:p.Asn1419=
NM_001083961.2:c.4257C>T MANE Select	NP_001077430.1:p.Asn1419=
NM_173636.5:c.4242C>T	NP_775907.4:p.Asn1414=