Canonical Allele Identifier: CA405452694

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593866C>T (hg19) ; chr19:g.36102964C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102964C>T , CM000681.2:g.36102964C>T	GRCh38
NC_000019.9:g.36593866C>T , CM000681.1:g.36593866C>T	GRCh37
NC_000019.8:g.41285706C>T	NCBI36
NG_028101.1:g.53084C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3337C>T	ENSP00000270301.6:p.Pro1113Ser
ENST00000401500.7:c.3352C>T MANE Select	ENSP00000384792.1:p.Pro1118Ser
ENST00000587391.6:c.*3212C>T	ENSP00000465525.1:n.*3212C>T
ENST00000679357.1:c.1432C>T
ENST00000679598.1:c.117C>T
ENST00000679682.1:c.3337C>T	ENSP00000506226.1:p.Pro1113Ser
ENST00000679714.1:c.3346C>T	ENSP00000506627.1:p.Pro1116Ser
ENST00000679757.1:c.3001C>T	ENSP00000505158.1:p.Pro1001Ser
ENST00000679858.1:c.*2734C>T	ENSP00000505655.1:n.*2734C>T
ENST00000680211.1:c.-48C>T	ENSP00000506102.1:n.-48C>T
ENST00000680280.1:n.639C>T
ENST00000680349.1:n.1920C>T
ENST00000680403.1:c.3337C>T	ENSP00000505677.1:p.Pro1113Ser
ENST00000680564.1:c.3103C>T	ENSP00000505582.1:p.Pro1035Ser
ENST00000680590.1:c.*1732C>T	ENSP00000505350.1:n.*1732C>T
ENST00000680597.1:c.117C>T
ENST00000680739.1:c.367C>T
ENST00000680773.1:n.1853C>T
ENST00000680806.1:c.*2655C>T	ENSP00000506418.1:n.*2655C>T
ENST00000680997.1:n.1284C>T
ENST00000681608.1:n.981C>T
ENST00000681625.1:c.*684C>T	ENSP00000505555.1:n.*684C>T
ENST00000681648.1:n.651C>T
ENST00000270301.11:c.3337C>T	ENSP00000270301.6:p.Pro1113Ser
ENST00000401500.6:c.3352C>T	ENSP00000384792.1:p.Pro1118Ser
ENST00000587391.5:c.*3212C>T	ENSP00000465525.1:n.*3212C>T
NM_001083961.1:c.3352C>T	NP_001077430.1:p.Pro1118Ser
NM_173636.4:c.3337C>T	NP_775907.4:p.Pro1113Ser
XM_005258809.2:c.3241C>T	XP_005258866.1:p.Pro1081Ser
XM_011526837.1:c.3337C>T	XP_011525139.1:p.Pro1113Ser
XM_011526838.1:c.3103C>T	XP_011525140.1:p.Pro1035Ser
XM_011526839.1:c.3001C>T	XP_011525141.1:p.Pro1001Ser
XM_011526840.1:c.2344C>T	XP_011525142.1:p.Pro782Ser
XM_011526841.1:c.1930C>T	XP_011525143.1:p.Pro644Ser
XM_011526842.1:c.1783C>T	XP_011525144.1:p.Pro595Ser
XM_011526843.1:c.1099C>T	XP_011525145.1:p.Pro367Ser
XM_011526844.1:c.1099C>T	XP_011525146.1:p.Pro367Ser
XM_011526840.2:c.2344C>T	XP_011525142.1:p.Pro782Ser
XM_011526841.2:c.1930C>T	XP_011525143.1:p.Pro644Ser
XM_011526844.2:c.1099C>T	XP_011525146.1:p.Pro367Ser
XM_017026665.1:c.3352C>T	XP_016882154.1:p.Pro1118Ser
NM_001083961.2:c.3352C>T MANE Select	NP_001077430.1:p.Pro1118Ser
NM_173636.5:c.3337C>T	NP_775907.4:p.Pro1113Ser