Canonical Allele Identifier: CA405460641

Gene: WDR62

Linked Data

• dbSNP Id: rs1973620143
• MyVariant Identifiers: chr19:g.36595477T>C (hg19) ; chr19:g.36104575T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104575T>C , CM000681.2:g.36104575T>C	GRCh38
NC_000019.9:g.36595477T>C , CM000681.1:g.36595477T>C	GRCh37
NC_000019.8:g.41287317T>C	NCBI36
NG_028101.1:g.54695T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4196T>C	ENSP00000270301.6:p.Val1399Ala
ENST00000401500.7:c.4211T>C MANE Select	ENSP00000384792.1:p.Val1404Ala
ENST00000587391.6:c.*4071T>C	ENSP00000465525.1:n.*4071T>C
ENST00000679357.1:c.2291T>C
ENST00000679598.1:c.956T>C
ENST00000679682.1:c.4196T>C	ENSP00000506226.1:p.Val1399Ala
ENST00000679714.1:c.4205T>C	ENSP00000506627.1:p.Val1402Ala
ENST00000679757.1:c.3860T>C	ENSP00000505158.1:p.Val1287Ala
ENST00000679858.1:c.*3593T>C	ENSP00000505655.1:n.*3593T>C
ENST00000680211.1:c.812T>C	ENSP00000506102.1:p.Val271Ala
ENST00000680280.1:n.1714T>C
ENST00000680349.1:n.2860T>C
ENST00000680403.1:c.4196T>C	ENSP00000505677.1:p.Val1399Ala
ENST00000680564.1:c.3962T>C	ENSP00000505582.1:p.Val1321Ala
ENST00000680590.1:c.*2591T>C	ENSP00000505350.1:n.*2591T>C
ENST00000680597.1:c.944T>C
ENST00000680739.1:c.1226T>C
ENST00000680773.1:n.2712T>C
ENST00000680806.1:c.*3514T>C	ENSP00000506418.1:n.*3514T>C
ENST00000680997.1:n.2143T>C
ENST00000681608.1:n.2056T>C
ENST00000681625.1:c.*1543T>C	ENSP00000505555.1:n.*1543T>C
ENST00000681648.1:n.2262T>C
ENST00000270301.11:c.4196T>C	ENSP00000270301.6:p.Val1399Ala
ENST00000401500.6:c.4211T>C	ENSP00000384792.1:p.Val1404Ala
ENST00000587391.5:c.*4071T>C	ENSP00000465525.1:n.*4071T>C
NM_001083961.1:c.4211T>C	NP_001077430.1:p.Val1404Ala
NM_173636.4:c.4196T>C	NP_775907.4:p.Val1399Ala
XM_005258809.2:c.4100T>C	XP_005258866.1:p.Val1367Ala
XM_011526837.1:c.4196T>C	XP_011525139.1:p.Val1399Ala
XM_011526838.1:c.3962T>C	XP_011525140.1:p.Val1321Ala
XM_011526839.1:c.3860T>C	XP_011525141.1:p.Val1287Ala
XM_011526840.1:c.3203T>C	XP_011525142.1:p.Val1068Ala
XM_011526841.1:c.2789T>C	XP_011525143.1:p.Val930Ala
XM_011526842.1:c.2642T>C	XP_011525144.1:p.Val881Ala
XM_011526843.1:c.1958T>C	XP_011525145.1:p.Val653Ala
XM_011526844.1:c.1958T>C	XP_011525146.1:p.Val653Ala
XM_011526840.2:c.3203T>C	XP_011525142.1:p.Val1068Ala
XM_011526841.2:c.2789T>C	XP_011525143.1:p.Val930Ala
XM_011526844.2:c.1958T>C	XP_011525146.1:p.Val653Ala
XM_017026665.1:c.4211T>C	XP_016882154.1:p.Val1404Ala
NM_001083961.2:c.4211T>C MANE Select	NP_001077430.1:p.Val1404Ala
NM_173636.5:c.4196T>C	NP_775907.4:p.Val1399Ala