Canonical Allele Identifier: CA405460611

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595473C>T (hg19) ; chr19:g.36104571C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104571C>T , CM000681.2:g.36104571C>T	GRCh38
NC_000019.9:g.36595473C>T , CM000681.1:g.36595473C>T	GRCh37
NC_000019.8:g.41287313C>T	NCBI36
NG_028101.1:g.54691C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4192C>T	ENSP00000270301.6:p.Pro1398Ser
ENST00000401500.7:c.4207C>T MANE Select	ENSP00000384792.1:p.Pro1403Ser
ENST00000587391.6:c.*4067C>T	ENSP00000465525.1:n.*4067C>T
ENST00000679357.1:c.2287C>T
ENST00000679598.1:c.952C>T
ENST00000679682.1:c.4192C>T	ENSP00000506226.1:p.Pro1398Ser
ENST00000679714.1:c.4201C>T	ENSP00000506627.1:p.Pro1401Ser
ENST00000679757.1:c.3856C>T	ENSP00000505158.1:p.Pro1286Ser
ENST00000679858.1:c.*3589C>T	ENSP00000505655.1:n.*3589C>T
ENST00000680211.1:c.808C>T	ENSP00000506102.1:p.Pro270Ser
ENST00000680280.1:n.1710C>T
ENST00000680349.1:n.2856C>T
ENST00000680403.1:c.4192C>T	ENSP00000505677.1:p.Pro1398Ser
ENST00000680564.1:c.3958C>T	ENSP00000505582.1:p.Pro1320Ser
ENST00000680590.1:c.*2587C>T	ENSP00000505350.1:n.*2587C>T
ENST00000680597.1:c.940C>T
ENST00000680739.1:c.1222C>T
ENST00000680773.1:n.2708C>T
ENST00000680806.1:c.*3510C>T	ENSP00000506418.1:n.*3510C>T
ENST00000680997.1:n.2139C>T
ENST00000681608.1:n.2052C>T
ENST00000681625.1:c.*1539C>T	ENSP00000505555.1:n.*1539C>T
ENST00000681648.1:n.2258C>T
ENST00000270301.11:c.4192C>T	ENSP00000270301.6:p.Pro1398Ser
ENST00000401500.6:c.4207C>T	ENSP00000384792.1:p.Pro1403Ser
ENST00000587391.5:c.*4067C>T	ENSP00000465525.1:n.*4067C>T
NM_001083961.1:c.4207C>T	NP_001077430.1:p.Pro1403Ser
NM_173636.4:c.4192C>T	NP_775907.4:p.Pro1398Ser
XM_005258809.2:c.4096C>T	XP_005258866.1:p.Pro1366Ser
XM_011526837.1:c.4192C>T	XP_011525139.1:p.Pro1398Ser
XM_011526838.1:c.3958C>T	XP_011525140.1:p.Pro1320Ser
XM_011526839.1:c.3856C>T	XP_011525141.1:p.Pro1286Ser
XM_011526840.1:c.3199C>T	XP_011525142.1:p.Pro1067Ser
XM_011526841.1:c.2785C>T	XP_011525143.1:p.Pro929Ser
XM_011526842.1:c.2638C>T	XP_011525144.1:p.Pro880Ser
XM_011526843.1:c.1954C>T	XP_011525145.1:p.Pro652Ser
XM_011526844.1:c.1954C>T	XP_011525146.1:p.Pro652Ser
XM_011526840.2:c.3199C>T	XP_011525142.1:p.Pro1067Ser
XM_011526841.2:c.2785C>T	XP_011525143.1:p.Pro929Ser
XM_011526844.2:c.1954C>T	XP_011525146.1:p.Pro652Ser
XM_017026665.1:c.4207C>T	XP_016882154.1:p.Pro1403Ser
NM_001083961.2:c.4207C>T MANE Select	NP_001077430.1:p.Pro1403Ser
NM_173636.5:c.4192C>T	NP_775907.4:p.Pro1398Ser