Canonical Allele Identifier: CA405460869

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595500C>T (hg19) ; chr19:g.36104598C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104598C>T , CM000681.2:g.36104598C>T	GRCh38
NC_000019.9:g.36595500C>T , CM000681.1:g.36595500C>T	GRCh37
NC_000019.8:g.41287340C>T	NCBI36
NG_028101.1:g.54718C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4219C>T	ENSP00000270301.6:p.Leu1407Phe
ENST00000401500.7:c.4234C>T MANE Select	ENSP00000384792.1:p.Leu1412Phe
ENST00000587391.6:c.*4094C>T	ENSP00000465525.1:n.*4094C>T
ENST00000679357.1:c.2314C>T
ENST00000679598.1:c.979C>T
ENST00000679682.1:c.4219C>T	ENSP00000506226.1:p.Leu1407Phe
ENST00000679714.1:c.4228C>T	ENSP00000506627.1:p.Leu1410Phe
ENST00000679757.1:c.3883C>T	ENSP00000505158.1:p.Leu1295Phe
ENST00000679858.1:c.*3616C>T	ENSP00000505655.1:n.*3616C>T
ENST00000680211.1:c.835C>T	ENSP00000506102.1:p.Leu279Phe
ENST00000680280.1:n.1737C>T
ENST00000680349.1:n.2883C>T
ENST00000680403.1:c.4219C>T	ENSP00000505677.1:p.Leu1407Phe
ENST00000680564.1:c.3985C>T	ENSP00000505582.1:p.Leu1329Phe
ENST00000680590.1:c.*2614C>T	ENSP00000505350.1:n.*2614C>T
ENST00000680597.1:c.967C>T
ENST00000680739.1:c.1249C>T
ENST00000680773.1:n.2735C>T
ENST00000680806.1:c.*3537C>T	ENSP00000506418.1:n.*3537C>T
ENST00000680997.1:n.2166C>T
ENST00000681608.1:n.2079C>T
ENST00000681625.1:c.*1566C>T	ENSP00000505555.1:n.*1566C>T
ENST00000681648.1:n.2285C>T
ENST00000270301.11:c.4219C>T	ENSP00000270301.6:p.Leu1407Phe
ENST00000401500.6:c.4234C>T	ENSP00000384792.1:p.Leu1412Phe
ENST00000587391.5:c.*4094C>T	ENSP00000465525.1:n.*4094C>T
NM_001083961.1:c.4234C>T	NP_001077430.1:p.Leu1412Phe
NM_173636.4:c.4219C>T	NP_775907.4:p.Leu1407Phe
XM_005258809.2:c.4123C>T	XP_005258866.1:p.Leu1375Phe
XM_011526837.1:c.4219C>T	XP_011525139.1:p.Leu1407Phe
XM_011526838.1:c.3985C>T	XP_011525140.1:p.Leu1329Phe
XM_011526839.1:c.3883C>T	XP_011525141.1:p.Leu1295Phe
XM_011526840.1:c.3226C>T	XP_011525142.1:p.Leu1076Phe
XM_011526841.1:c.2812C>T	XP_011525143.1:p.Leu938Phe
XM_011526842.1:c.2665C>T	XP_011525144.1:p.Leu889Phe
XM_011526843.1:c.1981C>T	XP_011525145.1:p.Leu661Phe
XM_011526844.1:c.1981C>T	XP_011525146.1:p.Leu661Phe
XM_011526840.2:c.3226C>T	XP_011525142.1:p.Leu1076Phe
XM_011526841.2:c.2812C>T	XP_011525143.1:p.Leu938Phe
XM_011526844.2:c.1981C>T	XP_011525146.1:p.Leu661Phe
XM_017026665.1:c.4234C>T	XP_016882154.1:p.Leu1412Phe
NM_001083961.2:c.4234C>T MANE Select	NP_001077430.1:p.Leu1412Phe
NM_173636.5:c.4219C>T	NP_775907.4:p.Leu1407Phe