Canonical Allele Identifier: CA507107502

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592938T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102036T>C , CM000681.2:g.36102036T>C	GRCh38
NC_000019.9:g.36592938T>C , CM000681.1:g.36592938T>C	GRCh37
NC_000019.8:g.41284778T>C	NCBI36
NG_028101.1:g.52156T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3105T>C	ENSP00000270301.6:p.Asp1035=
ENST00000401500.7:c.3105T>C MANE Select	ENSP00000384792.1:p.Asp1035=
ENST00000587391.6:c.*2380T>C	ENSP00000465525.1:n.*2380T>C
ENST00000679357.1:c.895T>C
ENST00000679422.1:c.784T>C
ENST00000679682.1:c.3090T>C	ENSP00000506226.1:p.Asp1030=
ENST00000679714.1:c.3099T>C	ENSP00000506627.1:p.Asp1033=
ENST00000679757.1:c.2754T>C	ENSP00000505158.1:p.Asp918=
ENST00000679858.1:c.*2487T>C	ENSP00000505655.1:n.*2487T>C
ENST00000680211.1:c.-295T>C	ENSP00000506102.1:n.-295T>C
ENST00000680349.1:n.1088T>C
ENST00000680403.1:c.3105T>C	ENSP00000505677.1:p.Asp1035=
ENST00000680564.1:c.2972-701T>C	ENSP00000505582.1:n.2972-701T>C
ENST00000680590.1:c.*1500T>C	ENSP00000505350.1:n.*1500T>C
ENST00000680739.1:c.23T>C
ENST00000680773.1:n.1021T>C
ENST00000680806.1:c.*1823T>C	ENSP00000506418.1:n.*1823T>C
ENST00000680997.1:n.452T>C
ENST00000681088.1:c.767T>C
ENST00000681608.1:n.53T>C
ENST00000681625.1:c.*437T>C	ENSP00000505555.1:n.*437T>C
ENST00000270301.11:c.3105T>C	ENSP00000270301.6:p.Asp1035=
ENST00000401500.6:c.3105T>C	ENSP00000384792.1:p.Asp1035=
ENST00000587391.5:c.*2380T>C	ENSP00000465525.1:n.*2380T>C
NM_001083961.1:c.3105T>C	NP_001077430.1:p.Asp1035=
NM_173636.4:c.3105T>C	NP_775907.4:p.Asp1035=
XM_005258809.2:c.2994T>C	XP_005258866.1:p.Asp998=
XM_011526837.1:c.3090T>C	XP_011525139.1:p.Asp1030=
XM_011526838.1:c.2972-701T>C	XP_011525140.1:n.2972-701T>C
XM_011526839.1:c.2754T>C	XP_011525141.1:p.Asp918=
XM_011526840.1:c.2097T>C	XP_011525142.1:p.Asp699=
XM_011526841.1:c.1683T>C	XP_011525143.1:p.Asp561=
XM_011526842.1:c.1536T>C	XP_011525144.1:p.Asp512=
XM_011526843.1:c.852T>C	XP_011525145.1:p.Asp284=
XM_011526844.1:c.852T>C	XP_011525146.1:p.Asp284=
XM_011526840.2:c.2097T>C	XP_011525142.1:p.Asp699=
XM_011526841.2:c.1683T>C	XP_011525143.1:p.Asp561=
XM_011526844.2:c.852T>C	XP_011525146.1:p.Asp284=
XM_017026665.1:c.3105T>C	XP_016882154.1:p.Asp1035=
NM_001083961.2:c.3105T>C MANE Select	NP_001077430.1:p.Asp1035=
NM_173636.5:c.3105T>C	NP_775907.4:p.Asp1035=