Canonical Allele Identifier: CA507107514

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102051-C-A
• MyVariant Identifiers: chr19:g.36592953C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102051C>A , CM000681.2:g.36102051C>A	GRCh38
NC_000019.9:g.36592953C>A , CM000681.1:g.36592953C>A	GRCh37
NC_000019.8:g.41284793C>A	NCBI36
NG_028101.1:g.52171C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3120C>A	ENSP00000270301.6:p.Pro1040=
ENST00000401500.7:c.3120C>A MANE Select	ENSP00000384792.1:p.Pro1040=
ENST00000587391.6:c.*2395C>A	ENSP00000465525.1:n.*2395C>A
ENST00000679357.1:c.910C>A
ENST00000679422.1:c.799C>A
ENST00000679682.1:c.3105C>A	ENSP00000506226.1:p.Pro1035=
ENST00000679714.1:c.3114C>A	ENSP00000506627.1:p.Pro1038=
ENST00000679757.1:c.2769C>A	ENSP00000505158.1:p.Pro923=
ENST00000679858.1:c.*2502C>A	ENSP00000505655.1:n.*2502C>A
ENST00000680211.1:c.-280C>A	ENSP00000506102.1:n.-280C>A
ENST00000680349.1:n.1103C>A
ENST00000680403.1:c.3120C>A	ENSP00000505677.1:p.Pro1040=
ENST00000680564.1:c.2972-686C>A	ENSP00000505582.1:n.2972-686C>A
ENST00000680590.1:c.*1515C>A	ENSP00000505350.1:n.*1515C>A
ENST00000680739.1:c.38C>A
ENST00000680773.1:n.1036C>A
ENST00000680806.1:c.*1838C>A	ENSP00000506418.1:n.*1838C>A
ENST00000680997.1:n.467C>A
ENST00000681088.1:c.782C>A
ENST00000681608.1:n.68C>A
ENST00000681625.1:c.*452C>A	ENSP00000505555.1:n.*452C>A
ENST00000270301.11:c.3120C>A	ENSP00000270301.6:p.Pro1040=
ENST00000401500.6:c.3120C>A	ENSP00000384792.1:p.Pro1040=
ENST00000587391.5:c.*2395C>A	ENSP00000465525.1:n.*2395C>A
NM_001083961.1:c.3120C>A	NP_001077430.1:p.Pro1040=
NM_173636.4:c.3120C>A	NP_775907.4:p.Pro1040=
XM_005258809.2:c.3009C>A	XP_005258866.1:p.Pro1003=
XM_011526837.1:c.3105C>A	XP_011525139.1:p.Pro1035=
XM_011526838.1:c.2972-686C>A	XP_011525140.1:n.2972-686C>A
XM_011526839.1:c.2769C>A	XP_011525141.1:p.Pro923=
XM_011526840.1:c.2112C>A	XP_011525142.1:p.Pro704=
XM_011526841.1:c.1698C>A	XP_011525143.1:p.Pro566=
XM_011526842.1:c.1551C>A	XP_011525144.1:p.Pro517=
XM_011526843.1:c.867C>A	XP_011525145.1:p.Pro289=
XM_011526844.1:c.867C>A	XP_011525146.1:p.Pro289=
XM_011526840.2:c.2112C>A	XP_011525142.1:p.Pro704=
XM_011526841.2:c.1698C>A	XP_011525143.1:p.Pro566=
XM_011526844.2:c.867C>A	XP_011525146.1:p.Pro289=
XM_017026665.1:c.3120C>A	XP_016882154.1:p.Pro1040=
NM_001083961.2:c.3120C>A MANE Select	NP_001077430.1:p.Pro1040=
NM_173636.5:c.3120C>A	NP_775907.4:p.Pro1040=