Canonical Allele Identifier: CA405460894

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595505G>C (hg19) ; chr19:g.36104603G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104603G>C , CM000681.2:g.36104603G>C	GRCh38
NC_000019.9:g.36595505G>C , CM000681.1:g.36595505G>C	GRCh37
NC_000019.8:g.41287345G>C	NCBI36
NG_028101.1:g.54723G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4224G>C	ENSP00000270301.6:p.Glu1408Asp
ENST00000401500.7:c.4239G>C MANE Select	ENSP00000384792.1:p.Glu1413Asp
ENST00000587391.6:c.*4099G>C	ENSP00000465525.1:n.*4099G>C
ENST00000679357.1:c.2319G>C
ENST00000679598.1:c.984G>C
ENST00000679682.1:c.4224G>C	ENSP00000506226.1:p.Glu1408Asp
ENST00000679714.1:c.4233G>C	ENSP00000506627.1:p.Glu1411Asp
ENST00000679757.1:c.3888G>C	ENSP00000505158.1:p.Glu1296Asp
ENST00000679858.1:c.*3621G>C	ENSP00000505655.1:n.*3621G>C
ENST00000680211.1:c.840G>C	ENSP00000506102.1:p.Glu280Asp
ENST00000680280.1:n.1742G>C
ENST00000680349.1:n.2888G>C
ENST00000680403.1:c.4224G>C	ENSP00000505677.1:p.Glu1408Asp
ENST00000680564.1:c.3990G>C	ENSP00000505582.1:p.Glu1330Asp
ENST00000680590.1:c.*2619G>C	ENSP00000505350.1:n.*2619G>C
ENST00000680597.1:c.972G>C
ENST00000680739.1:c.1254G>C
ENST00000680773.1:n.2740G>C
ENST00000680806.1:c.*3542G>C	ENSP00000506418.1:n.*3542G>C
ENST00000680997.1:n.2171G>C
ENST00000681608.1:n.2084G>C
ENST00000681625.1:c.*1571G>C	ENSP00000505555.1:n.*1571G>C
ENST00000681648.1:n.2290G>C
ENST00000270301.11:c.4224G>C	ENSP00000270301.6:p.Glu1408Asp
ENST00000401500.6:c.4239G>C	ENSP00000384792.1:p.Glu1413Asp
ENST00000587391.5:c.*4099G>C	ENSP00000465525.1:n.*4099G>C
NM_001083961.1:c.4239G>C	NP_001077430.1:p.Glu1413Asp
NM_173636.4:c.4224G>C	NP_775907.4:p.Glu1408Asp
XM_005258809.2:c.4128G>C	XP_005258866.1:p.Glu1376Asp
XM_011526837.1:c.4224G>C	XP_011525139.1:p.Glu1408Asp
XM_011526838.1:c.3990G>C	XP_011525140.1:p.Glu1330Asp
XM_011526839.1:c.3888G>C	XP_011525141.1:p.Glu1296Asp
XM_011526840.1:c.3231G>C	XP_011525142.1:p.Glu1077Asp
XM_011526841.1:c.2817G>C	XP_011525143.1:p.Glu939Asp
XM_011526842.1:c.2670G>C	XP_011525144.1:p.Glu890Asp
XM_011526843.1:c.1986G>C	XP_011525145.1:p.Glu662Asp
XM_011526844.1:c.1986G>C	XP_011525146.1:p.Glu662Asp
XM_011526840.2:c.3231G>C	XP_011525142.1:p.Glu1077Asp
XM_011526841.2:c.2817G>C	XP_011525143.1:p.Glu939Asp
XM_011526844.2:c.1986G>C	XP_011525146.1:p.Glu662Asp
XM_017026665.1:c.4239G>C	XP_016882154.1:p.Glu1413Asp
NM_001083961.2:c.4239G>C MANE Select	NP_001077430.1:p.Glu1413Asp
NM_173636.5:c.4224G>C	NP_775907.4:p.Glu1408Asp