Canonical Allele Identifier: CA405457520

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36594452T>A (hg19) ; chr19:g.36103550T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36103550T>A , CM000681.2:g.36103550T>A	GRCh38
NC_000019.9:g.36594452T>A , CM000681.1:g.36594452T>A	GRCh37
NC_000019.8:g.41286292T>A	NCBI36
NG_028101.1:g.53670T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3707T>A	ENSP00000270301.6:p.Ile1236Asn
ENST00000401500.7:c.3722T>A MANE Select	ENSP00000384792.1:p.Ile1241Asn
ENST00000587391.6:c.*3582T>A	ENSP00000465525.1:n.*3582T>A
ENST00000679357.1:c.1802T>A
ENST00000679598.1:c.487T>A
ENST00000679682.1:c.3707T>A	ENSP00000506226.1:p.Ile1236Asn
ENST00000679714.1:c.3716T>A	ENSP00000506627.1:p.Ile1239Asn
ENST00000679757.1:c.3371T>A	ENSP00000505158.1:p.Ile1124Asn
ENST00000679858.1:c.*3104T>A	ENSP00000505655.1:n.*3104T>A
ENST00000680211.1:c.323T>A	ENSP00000506102.1:p.Ile108Asn
ENST00000680280.1:n.1225T>A
ENST00000680349.1:n.2371T>A
ENST00000680403.1:c.3707T>A	ENSP00000505677.1:p.Ile1236Asn
ENST00000680564.1:c.3473T>A	ENSP00000505582.1:p.Ile1158Asn
ENST00000680590.1:c.*2102T>A	ENSP00000505350.1:n.*2102T>A
ENST00000680597.1:c.455T>A
ENST00000680739.1:c.737T>A
ENST00000680773.1:n.2223T>A
ENST00000680806.1:c.*3025T>A	ENSP00000506418.1:n.*3025T>A
ENST00000680997.1:n.1654T>A
ENST00000681608.1:n.1567T>A
ENST00000681625.1:c.*1054T>A	ENSP00000505555.1:n.*1054T>A
ENST00000681648.1:n.1237T>A
ENST00000270301.11:c.3707T>A	ENSP00000270301.6:p.Ile1236Asn
ENST00000401500.6:c.3722T>A	ENSP00000384792.1:p.Ile1241Asn
ENST00000587391.5:c.*3582T>A	ENSP00000465525.1:n.*3582T>A
NM_001083961.1:c.3722T>A	NP_001077430.1:p.Ile1241Asn
NM_173636.4:c.3707T>A	NP_775907.4:p.Ile1236Asn
XM_005258809.2:c.3611T>A	XP_005258866.1:p.Ile1204Asn
XM_011526837.1:c.3707T>A	XP_011525139.1:p.Ile1236Asn
XM_011526838.1:c.3473T>A	XP_011525140.1:p.Ile1158Asn
XM_011526839.1:c.3371T>A	XP_011525141.1:p.Ile1124Asn
XM_011526840.1:c.2714T>A	XP_011525142.1:p.Ile905Asn
XM_011526841.1:c.2300T>A	XP_011525143.1:p.Ile767Asn
XM_011526842.1:c.2153T>A	XP_011525144.1:p.Ile718Asn
XM_011526843.1:c.1469T>A	XP_011525145.1:p.Ile490Asn
XM_011526844.1:c.1469T>A	XP_011525146.1:p.Ile490Asn
XM_011526840.2:c.2714T>A	XP_011525142.1:p.Ile905Asn
XM_011526841.2:c.2300T>A	XP_011525143.1:p.Ile767Asn
XM_011526844.2:c.1469T>A	XP_011525146.1:p.Ile490Asn
XM_017026665.1:c.3722T>A	XP_016882154.1:p.Ile1241Asn
NM_001083961.2:c.3722T>A MANE Select	NP_001077430.1:p.Ile1241Asn
NM_173636.5:c.3707T>A	NP_775907.4:p.Ile1236Asn