Canonical Allele Identifier: CA405461192

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595534G>T (hg19) ; chr19:g.36104632G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104632G>T , CM000681.2:g.36104632G>T	GRCh38
NC_000019.9:g.36595534G>T , CM000681.1:g.36595534G>T	GRCh37
NC_000019.8:g.41287374G>T	NCBI36
NG_028101.1:g.54752G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4253G>T	ENSP00000270301.6:p.Arg1418Met
ENST00000401500.7:c.4268G>T MANE Select	ENSP00000384792.1:p.Arg1423Met
ENST00000587391.6:c.*4128G>T	ENSP00000465525.1:n.*4128G>T
ENST00000679357.1:c.2348G>T
ENST00000679598.1:c.1013G>T
ENST00000679682.1:c.4253G>T	ENSP00000506226.1:p.Arg1418Met
ENST00000679714.1:c.4262G>T	ENSP00000506627.1:p.Arg1421Met
ENST00000679757.1:c.3917G>T	ENSP00000505158.1:p.Arg1306Met
ENST00000679858.1:c.*3650G>T	ENSP00000505655.1:n.*3650G>T
ENST00000680211.1:c.869G>T	ENSP00000506102.1:p.Arg290Met
ENST00000680280.1:n.1771G>T
ENST00000680349.1:n.2917G>T
ENST00000680403.1:c.4253G>T	ENSP00000505677.1:p.Arg1418Met
ENST00000680564.1:c.4019G>T	ENSP00000505582.1:p.Arg1340Met
ENST00000680590.1:c.*2648G>T	ENSP00000505350.1:n.*2648G>T
ENST00000680597.1:c.1001G>T
ENST00000680739.1:c.1283G>T
ENST00000680773.1:n.2769G>T
ENST00000680806.1:c.*3571G>T	ENSP00000506418.1:n.*3571G>T
ENST00000680997.1:n.2200G>T
ENST00000681608.1:n.2113G>T
ENST00000681625.1:c.*1600G>T	ENSP00000505555.1:n.*1600G>T
ENST00000681648.1:n.2319G>T
ENST00000270301.11:c.4253G>T	ENSP00000270301.6:p.Arg1418Met
ENST00000401500.6:c.4268G>T	ENSP00000384792.1:p.Arg1423Met
ENST00000587391.5:c.*4128G>T	ENSP00000465525.1:n.*4128G>T
NM_001083961.1:c.4268G>T	NP_001077430.1:p.Arg1423Met
NM_173636.4:c.4253G>T	NP_775907.4:p.Arg1418Met
XM_005258809.2:c.4157G>T	XP_005258866.1:p.Arg1386Met
XM_011526837.1:c.4253G>T	XP_011525139.1:p.Arg1418Met
XM_011526838.1:c.4019G>T	XP_011525140.1:p.Arg1340Met
XM_011526839.1:c.3917G>T	XP_011525141.1:p.Arg1306Met
XM_011526840.1:c.3260G>T	XP_011525142.1:p.Arg1087Met
XM_011526841.1:c.2846G>T	XP_011525143.1:p.Arg949Met
XM_011526842.1:c.2699G>T	XP_011525144.1:p.Arg900Met
XM_011526843.1:c.2015G>T	XP_011525145.1:p.Arg672Met
XM_011526844.1:c.2015G>T	XP_011525146.1:p.Arg672Met
XM_011526840.2:c.3260G>T	XP_011525142.1:p.Arg1087Met
XM_011526841.2:c.2846G>T	XP_011525143.1:p.Arg949Met
XM_011526844.2:c.2015G>T	XP_011525146.1:p.Arg672Met
XM_017026665.1:c.4268G>T	XP_016882154.1:p.Arg1423Met
NM_001083961.2:c.4268G>T MANE Select	NP_001077430.1:p.Arg1423Met
NM_173636.5:c.4253G>T	NP_775907.4:p.Arg1418Met