Canonical Allele Identifier: CA633062297

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36073473_36073498dup , CM000681.2:g.36073473_36073498dup	GRCh38
NC_000019.9:g.36564375_36564400dup , CM000681.1:g.36564375_36564400dup	GRCh37
NC_000019.8:g.41256215_41256240dup	NCBI36
NG_028101.1:g.23593_23618dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.1175_1200dup	ENSP00000270301.6:p.Leu401ThrfsTer38
ENST00000401500.7:c.1175_1200dup MANE Select	ENSP00000384792.1:p.Leu401ThrfsTer38
ENST00000587391.6:c.1175_1200dup	ENSP00000465525.1:p.Leu401ThrfsTer38
ENST00000589953.2:n.1480_1505dup
ENST00000644764.2:c.1175_1200dup	ENSP00000494253.2:p.Leu401ThrfsTer?
ENST00000679682.1:c.1160_1185dup	ENSP00000506226.1:p.Leu396ThrfsTer38
ENST00000679714.1:c.1175_1200dup	ENSP00000506627.1:p.Leu401ThrfsTer36
ENST00000679757.1:c.882+5463_882+5488dup	ENSP00000505158.1:n.882+5463_882+5488dup
ENST00000679858.1:c.*39_*64dup	ENSP00000505655.1:n.*39_*64dup
ENST00000680321.1:c.1160_1185dup	ENSP00000505525.1:p.Leu396ThrfsTer?
ENST00000680359.1:c.1175_1200dup	ENSP00000506079.1:p.Leu401ThrfsTer38
ENST00000680403.1:c.1175_1200dup	ENSP00000505677.1:p.Leu401ThrfsTer38
ENST00000680489.1:n.1498_1523dup
ENST00000680564.1:c.1175_1200dup	ENSP00000505582.1:p.Leu401ThrfsTer38
ENST00000680590.1:c.1175_1200dup	ENSP00000505350.1:p.Leu401ThrfsTer38
ENST00000680806.1:c.1175_1200dup	ENSP00000506418.1:p.Leu401ThrfsTer?
ENST00000681542.1:c.1175_1200dup	ENSP00000505251.1:p.Leu401ThrfsTer?
ENST00000681625.1:c.1160_1185dup	ENSP00000505555.1:p.Leu396ThrfsTer38
ENST00000270301.11:c.1175_1200dup	ENSP00000270301.6:p.Leu401ThrfsTer38
ENST00000378860.8:n.1266_1291dup
ENST00000401500.6:c.1175_1200dup	ENSP00000384792.1:p.Leu401ThrfsTer38
ENST00000587391.5:c.1175_1200dup	ENSP00000465525.1:p.Leu401ThrfsTer38
ENST00000589953.1:n.243_268dup
NM_001083961.1:c.1175_1200dup	NP_001077430.1:p.Leu401ThrfsTer38
NM_173636.4:c.1175_1200dup	NP_775907.4:p.Leu401ThrfsTer38
XM_005258809.2:c.1175_1200dup	XP_005258866.1:p.Leu401ThrfsTer38
XM_011526837.1:c.1160_1185dup	XP_011525139.1:p.Leu396ThrfsTer38
XM_011526838.1:c.1175_1200dup	XP_011525140.1:p.Leu401ThrfsTer38
XM_011526839.1:c.882+5463_882+5488dup	XP_011525141.1:n.882+5463_882+5488dup
XM_011526840.1:c.16_41dup	XP_011525142.1:p.Ser14ArgfsTer26
XM_011526840.2:c.16_41dup	XP_011525142.1:p.Ser14ArgfsTer26
XM_017026665.1:c.1175_1200dup	XP_016882154.1:p.Leu401ThrfsTer38
XR_001753671.1:n.1266_1291dup
XR_001753672.1:n.1266_1291dup
NM_001083961.2:c.1175_1200dup MANE Select	NP_001077430.1:p.Leu401ThrfsTer38
NM_173636.5:c.1175_1200dup	NP_775907.4:p.Leu401ThrfsTer38