Canonical Allele Identifier: CA405461027

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595521A>C (hg19) ; chr19:g.36104619A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104619A>C , CM000681.2:g.36104619A>C	GRCh38
NC_000019.9:g.36595521A>C , CM000681.1:g.36595521A>C	GRCh37
NC_000019.8:g.41287361A>C	NCBI36
NG_028101.1:g.54739A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4240A>C	ENSP00000270301.6:p.Asn1414His
ENST00000401500.7:c.4255A>C MANE Select	ENSP00000384792.1:p.Asn1419His
ENST00000587391.6:c.*4115A>C	ENSP00000465525.1:n.*4115A>C
ENST00000679357.1:c.2335A>C
ENST00000679598.1:c.1000A>C
ENST00000679682.1:c.4240A>C	ENSP00000506226.1:p.Asn1414His
ENST00000679714.1:c.4249A>C	ENSP00000506627.1:p.Asn1417His
ENST00000679757.1:c.3904A>C	ENSP00000505158.1:p.Asn1302His
ENST00000679858.1:c.*3637A>C	ENSP00000505655.1:n.*3637A>C
ENST00000680211.1:c.856A>C	ENSP00000506102.1:p.Asn286His
ENST00000680280.1:n.1758A>C
ENST00000680349.1:n.2904A>C
ENST00000680403.1:c.4240A>C	ENSP00000505677.1:p.Asn1414His
ENST00000680564.1:c.4006A>C	ENSP00000505582.1:p.Asn1336His
ENST00000680590.1:c.*2635A>C	ENSP00000505350.1:n.*2635A>C
ENST00000680597.1:c.988A>C
ENST00000680739.1:c.1270A>C
ENST00000680773.1:n.2756A>C
ENST00000680806.1:c.*3558A>C	ENSP00000506418.1:n.*3558A>C
ENST00000680997.1:n.2187A>C
ENST00000681608.1:n.2100A>C
ENST00000681625.1:c.*1587A>C	ENSP00000505555.1:n.*1587A>C
ENST00000681648.1:n.2306A>C
ENST00000270301.11:c.4240A>C	ENSP00000270301.6:p.Asn1414His
ENST00000401500.6:c.4255A>C	ENSP00000384792.1:p.Asn1419His
ENST00000587391.5:c.*4115A>C	ENSP00000465525.1:n.*4115A>C
NM_001083961.1:c.4255A>C	NP_001077430.1:p.Asn1419His
NM_173636.4:c.4240A>C	NP_775907.4:p.Asn1414His
XM_005258809.2:c.4144A>C	XP_005258866.1:p.Asn1382His
XM_011526837.1:c.4240A>C	XP_011525139.1:p.Asn1414His
XM_011526838.1:c.4006A>C	XP_011525140.1:p.Asn1336His
XM_011526839.1:c.3904A>C	XP_011525141.1:p.Asn1302His
XM_011526840.1:c.3247A>C	XP_011525142.1:p.Asn1083His
XM_011526841.1:c.2833A>C	XP_011525143.1:p.Asn945His
XM_011526842.1:c.2686A>C	XP_011525144.1:p.Asn896His
XM_011526843.1:c.2002A>C	XP_011525145.1:p.Asn668His
XM_011526844.1:c.2002A>C	XP_011525146.1:p.Asn668His
XM_011526840.2:c.3247A>C	XP_011525142.1:p.Asn1083His
XM_011526841.2:c.2833A>C	XP_011525143.1:p.Asn945His
XM_011526844.2:c.2002A>C	XP_011525146.1:p.Asn668His
XM_017026665.1:c.4255A>C	XP_016882154.1:p.Asn1419His
NM_001083961.2:c.4255A>C MANE Select	NP_001077430.1:p.Asn1419His
NM_173636.5:c.4240A>C	NP_775907.4:p.Asn1414His