Canonical Allele Identifier: CA507107642

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593703A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102801A>C , CM000681.2:g.36102801A>C	GRCh38
NC_000019.9:g.36593703A>C , CM000681.1:g.36593703A>C	GRCh37
NC_000019.8:g.41285543A>C	NCBI36
NG_028101.1:g.52921A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3270A>C	ENSP00000270301.6:p.Pro1090=
ENST00000401500.7:c.3285A>C MANE Select	ENSP00000384792.1:p.Pro1095=
ENST00000587391.6:c.*3145A>C	ENSP00000465525.1:n.*3145A>C
ENST00000679357.1:c.1365A>C
ENST00000679598.1:c.50A>C
ENST00000679682.1:c.3270A>C	ENSP00000506226.1:p.Pro1090=
ENST00000679714.1:c.3279A>C	ENSP00000506627.1:p.Pro1093=
ENST00000679757.1:c.2934A>C	ENSP00000505158.1:p.Pro978=
ENST00000679858.1:c.*2667A>C	ENSP00000505655.1:n.*2667A>C
ENST00000680211.1:c.-115A>C	ENSP00000506102.1:n.-115A>C
ENST00000680280.1:n.572A>C
ENST00000680349.1:n.1853A>C
ENST00000680403.1:c.3270A>C	ENSP00000505677.1:p.Pro1090=
ENST00000680564.1:c.3036A>C	ENSP00000505582.1:p.Pro1012=
ENST00000680590.1:c.*1665A>C	ENSP00000505350.1:n.*1665A>C
ENST00000680597.1:c.50A>C
ENST00000680739.1:c.300A>C
ENST00000680773.1:n.1786A>C
ENST00000680806.1:c.*2588A>C	ENSP00000506418.1:n.*2588A>C
ENST00000680997.1:n.1217A>C
ENST00000681608.1:n.818A>C
ENST00000681625.1:c.*617A>C	ENSP00000505555.1:n.*617A>C
ENST00000681648.1:n.584A>C
ENST00000270301.11:c.3270A>C	ENSP00000270301.6:p.Pro1090=
ENST00000401500.6:c.3285A>C	ENSP00000384792.1:p.Pro1095=
ENST00000587391.5:c.*3145A>C	ENSP00000465525.1:n.*3145A>C
NM_001083961.1:c.3285A>C	NP_001077430.1:p.Pro1095=
NM_173636.4:c.3270A>C	NP_775907.4:p.Pro1090=
XM_005258809.2:c.3174A>C	XP_005258866.1:p.Pro1058=
XM_011526837.1:c.3270A>C	XP_011525139.1:p.Pro1090=
XM_011526838.1:c.3036A>C	XP_011525140.1:p.Pro1012=
XM_011526839.1:c.2934A>C	XP_011525141.1:p.Pro978=
XM_011526840.1:c.2277A>C	XP_011525142.1:p.Pro759=
XM_011526841.1:c.1863A>C	XP_011525143.1:p.Pro621=
XM_011526842.1:c.1716A>C	XP_011525144.1:p.Pro572=
XM_011526843.1:c.1032A>C	XP_011525145.1:p.Pro344=
XM_011526844.1:c.1032A>C	XP_011525146.1:p.Pro344=
XM_011526840.2:c.2277A>C	XP_011525142.1:p.Pro759=
XM_011526841.2:c.1863A>C	XP_011525143.1:p.Pro621=
XM_011526844.2:c.1032A>C	XP_011525146.1:p.Pro344=
XM_017026665.1:c.3285A>C	XP_016882154.1:p.Pro1095=
NM_001083961.2:c.3285A>C MANE Select	NP_001077430.1:p.Pro1095=
NM_173636.5:c.3270A>C	NP_775907.4:p.Pro1090=