Canonical Allele Identifier: CA507107565

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592995G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102093G>T , CM000681.2:g.36102093G>T	GRCh38
NC_000019.9:g.36592995G>T , CM000681.1:g.36592995G>T	GRCh37
NC_000019.8:g.41284835G>T	NCBI36
NG_028101.1:g.52213G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3162G>T	ENSP00000270301.6:p.Pro1054=
ENST00000401500.7:c.3162G>T MANE Select	ENSP00000384792.1:p.Pro1054=
ENST00000587391.6:c.*2437G>T	ENSP00000465525.1:n.*2437G>T
ENST00000679357.1:c.952G>T
ENST00000679422.1:c.841G>T
ENST00000679682.1:c.3147G>T	ENSP00000506226.1:p.Pro1049=
ENST00000679714.1:c.3156G>T	ENSP00000506627.1:p.Pro1052=
ENST00000679757.1:c.2811G>T	ENSP00000505158.1:p.Pro937=
ENST00000679858.1:c.*2544G>T	ENSP00000505655.1:n.*2544G>T
ENST00000680211.1:c.-238G>T	ENSP00000506102.1:n.-238G>T
ENST00000680349.1:n.1145G>T
ENST00000680403.1:c.3162G>T	ENSP00000505677.1:p.Pro1054=
ENST00000680564.1:c.2972-644G>T	ENSP00000505582.1:n.2972-644G>T
ENST00000680590.1:c.*1557G>T	ENSP00000505350.1:n.*1557G>T
ENST00000680739.1:c.80G>T
ENST00000680773.1:n.1078G>T
ENST00000680806.1:c.*1880G>T	ENSP00000506418.1:n.*1880G>T
ENST00000680997.1:n.509G>T
ENST00000681088.1:c.824G>T
ENST00000681608.1:n.110G>T
ENST00000681625.1:c.*494G>T	ENSP00000505555.1:n.*494G>T
ENST00000270301.11:c.3162G>T	ENSP00000270301.6:p.Pro1054=
ENST00000401500.6:c.3162G>T	ENSP00000384792.1:p.Pro1054=
ENST00000587391.5:c.*2437G>T	ENSP00000465525.1:n.*2437G>T
NM_001083961.1:c.3162G>T	NP_001077430.1:p.Pro1054=
NM_173636.4:c.3162G>T	NP_775907.4:p.Pro1054=
XM_005258809.2:c.3051G>T	XP_005258866.1:p.Pro1017=
XM_011526837.1:c.3147G>T	XP_011525139.1:p.Pro1049=
XM_011526838.1:c.2972-644G>T	XP_011525140.1:n.2972-644G>T
XM_011526839.1:c.2811G>T	XP_011525141.1:p.Pro937=
XM_011526840.1:c.2154G>T	XP_011525142.1:p.Pro718=
XM_011526841.1:c.1740G>T	XP_011525143.1:p.Pro580=
XM_011526842.1:c.1593G>T	XP_011525144.1:p.Pro531=
XM_011526843.1:c.909G>T	XP_011525145.1:p.Pro303=
XM_011526844.1:c.909G>T	XP_011525146.1:p.Pro303=
XM_011526840.2:c.2154G>T	XP_011525142.1:p.Pro718=
XM_011526841.2:c.1740G>T	XP_011525143.1:p.Pro580=
XM_011526844.2:c.909G>T	XP_011525146.1:p.Pro303=
XM_017026665.1:c.3162G>T	XP_016882154.1:p.Pro1054=
NM_001083961.2:c.3162G>T MANE Select	NP_001077430.1:p.Pro1054=
NM_173636.5:c.3162G>T	NP_775907.4:p.Pro1054=