Canonical Allele Identifier: CA405450567

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593007G>C (hg19) ; chr19:g.36102105G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102105G>C , CM000681.2:g.36102105G>C	GRCh38
NC_000019.9:g.36593007G>C , CM000681.1:g.36593007G>C	GRCh37
NC_000019.8:g.41284847G>C	NCBI36
NG_028101.1:g.52225G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3174G>C	ENSP00000270301.6:p.Lys1058Asn
ENST00000401500.7:c.3174G>C MANE Select	ENSP00000384792.1:p.Lys1058Asn
ENST00000587391.6:c.*2449G>C	ENSP00000465525.1:n.*2449G>C
ENST00000679357.1:c.964G>C
ENST00000679422.1:c.853G>C
ENST00000679682.1:c.3159G>C	ENSP00000506226.1:p.Lys1053Asn
ENST00000679714.1:c.3168G>C	ENSP00000506627.1:p.Lys1056Asn
ENST00000679757.1:c.2823G>C	ENSP00000505158.1:p.Lys941Asn
ENST00000679858.1:c.*2556G>C	ENSP00000505655.1:n.*2556G>C
ENST00000680211.1:c.-226G>C	ENSP00000506102.1:n.-226G>C
ENST00000680349.1:n.1157G>C
ENST00000680403.1:c.3174G>C	ENSP00000505677.1:p.Lys1058Asn
ENST00000680564.1:c.2972-632G>C	ENSP00000505582.1:n.2972-632G>C
ENST00000680590.1:c.*1569G>C	ENSP00000505350.1:n.*1569G>C
ENST00000680739.1:c.92G>C
ENST00000680773.1:n.1090G>C
ENST00000680806.1:c.*1892G>C	ENSP00000506418.1:n.*1892G>C
ENST00000680997.1:n.521G>C
ENST00000681088.1:c.836G>C
ENST00000681608.1:n.122G>C
ENST00000681625.1:c.*506G>C	ENSP00000505555.1:n.*506G>C
ENST00000270301.11:c.3174G>C	ENSP00000270301.6:p.Lys1058Asn
ENST00000401500.6:c.3174G>C	ENSP00000384792.1:p.Lys1058Asn
ENST00000587391.5:c.*2449G>C	ENSP00000465525.1:n.*2449G>C
NM_001083961.1:c.3174G>C	NP_001077430.1:p.Lys1058Asn
NM_173636.4:c.3174G>C	NP_775907.4:p.Lys1058Asn
XM_005258809.2:c.3063G>C	XP_005258866.1:p.Lys1021Asn
XM_011526837.1:c.3159G>C	XP_011525139.1:p.Lys1053Asn
XM_011526838.1:c.2972-632G>C	XP_011525140.1:n.2972-632G>C
XM_011526839.1:c.2823G>C	XP_011525141.1:p.Lys941Asn
XM_011526840.1:c.2166G>C	XP_011525142.1:p.Lys722Asn
XM_011526841.1:c.1752G>C	XP_011525143.1:p.Lys584Asn
XM_011526842.1:c.1605G>C	XP_011525144.1:p.Lys535Asn
XM_011526843.1:c.921G>C	XP_011525145.1:p.Lys307Asn
XM_011526844.1:c.921G>C	XP_011525146.1:p.Lys307Asn
XM_011526840.2:c.2166G>C	XP_011525142.1:p.Lys722Asn
XM_011526841.2:c.1752G>C	XP_011525143.1:p.Lys584Asn
XM_011526844.2:c.921G>C	XP_011525146.1:p.Lys307Asn
XM_017026665.1:c.3174G>C	XP_016882154.1:p.Lys1058Asn
NM_001083961.2:c.3174G>C MANE Select	NP_001077430.1:p.Lys1058Asn
NM_173636.5:c.3174G>C	NP_775907.4:p.Lys1058Asn