Canonical Allele Identifier: CA405461019

Gene: WDR62

Linked Data

• dbSNP Id: rs1973624937
• MyVariant Identifiers: chr19:g.36595519G>C (hg19) ; chr19:g.36104617G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104617G>C , CM000681.2:g.36104617G>C	GRCh38
NC_000019.9:g.36595519G>C , CM000681.1:g.36595519G>C	GRCh37
NC_000019.8:g.41287359G>C	NCBI36
NG_028101.1:g.54737G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4238G>C	ENSP00000270301.6:p.Gly1413Ala
ENST00000401500.7:c.4253G>C MANE Select	ENSP00000384792.1:p.Gly1418Ala
ENST00000587391.6:c.*4113G>C	ENSP00000465525.1:n.*4113G>C
ENST00000679357.1:c.2333G>C
ENST00000679598.1:c.998G>C
ENST00000679682.1:c.4238G>C	ENSP00000506226.1:p.Gly1413Ala
ENST00000679714.1:c.4247G>C	ENSP00000506627.1:p.Gly1416Ala
ENST00000679757.1:c.3902G>C	ENSP00000505158.1:p.Gly1301Ala
ENST00000679858.1:c.*3635G>C	ENSP00000505655.1:n.*3635G>C
ENST00000680211.1:c.854G>C	ENSP00000506102.1:p.Gly285Ala
ENST00000680280.1:n.1756G>C
ENST00000680349.1:n.2902G>C
ENST00000680403.1:c.4238G>C	ENSP00000505677.1:p.Gly1413Ala
ENST00000680564.1:c.4004G>C	ENSP00000505582.1:p.Gly1335Ala
ENST00000680590.1:c.*2633G>C	ENSP00000505350.1:n.*2633G>C
ENST00000680597.1:c.986G>C
ENST00000680739.1:c.1268G>C
ENST00000680773.1:n.2754G>C
ENST00000680806.1:c.*3556G>C	ENSP00000506418.1:n.*3556G>C
ENST00000680997.1:n.2185G>C
ENST00000681608.1:n.2098G>C
ENST00000681625.1:c.*1585G>C	ENSP00000505555.1:n.*1585G>C
ENST00000681648.1:n.2304G>C
ENST00000270301.11:c.4238G>C	ENSP00000270301.6:p.Gly1413Ala
ENST00000401500.6:c.4253G>C	ENSP00000384792.1:p.Gly1418Ala
ENST00000587391.5:c.*4113G>C	ENSP00000465525.1:n.*4113G>C
NM_001083961.1:c.4253G>C	NP_001077430.1:p.Gly1418Ala
NM_173636.4:c.4238G>C	NP_775907.4:p.Gly1413Ala
XM_005258809.2:c.4142G>C	XP_005258866.1:p.Gly1381Ala
XM_011526837.1:c.4238G>C	XP_011525139.1:p.Gly1413Ala
XM_011526838.1:c.4004G>C	XP_011525140.1:p.Gly1335Ala
XM_011526839.1:c.3902G>C	XP_011525141.1:p.Gly1301Ala
XM_011526840.1:c.3245G>C	XP_011525142.1:p.Gly1082Ala
XM_011526841.1:c.2831G>C	XP_011525143.1:p.Gly944Ala
XM_011526842.1:c.2684G>C	XP_011525144.1:p.Gly895Ala
XM_011526843.1:c.2000G>C	XP_011525145.1:p.Gly667Ala
XM_011526844.1:c.2000G>C	XP_011525146.1:p.Gly667Ala
XM_011526840.2:c.3245G>C	XP_011525142.1:p.Gly1082Ala
XM_011526841.2:c.2831G>C	XP_011525143.1:p.Gly944Ala
XM_011526844.2:c.2000G>C	XP_011525146.1:p.Gly667Ala
XM_017026665.1:c.4253G>C	XP_016882154.1:p.Gly1418Ala
NM_001083961.2:c.4253G>C MANE Select	NP_001077430.1:p.Gly1418Ala
NM_173636.5:c.4238G>C	NP_775907.4:p.Gly1413Ala