Canonical Allele Identifier: CA9396371

Gene: WDR62

Linked Data

• dbSNP Id: rs775723707
• ExAC: 19:36594453 C / T
• gnomAD v2: 19-36594453-C-T
• gnomAD v3: 19-36103551-C-T
• gnomAD v4: 19-36103551-C-T
• MyVariant Identifiers: chr19:g.36594453C>T (hg19) ; chr19:g.36103551C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36103551C>T , CM000681.2:g.36103551C>T	GRCh38
NC_000019.9:g.36594453C>T , CM000681.1:g.36594453C>T	GRCh37
NC_000019.8:g.41286293C>T	NCBI36
NG_028101.1:g.53671C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3708C>T	ENSP00000270301.6:p.Ile1236=
ENST00000401500.7:c.3723C>T MANE Select	ENSP00000384792.1:p.Ile1241=
ENST00000587391.6:c.*3583C>T	ENSP00000465525.1:n.*3583C>T
ENST00000679357.1:c.1803C>T
ENST00000679598.1:c.488C>T
ENST00000679682.1:c.3708C>T	ENSP00000506226.1:p.Ile1236=
ENST00000679714.1:c.3717C>T	ENSP00000506627.1:p.Ile1239=
ENST00000679757.1:c.3372C>T	ENSP00000505158.1:p.Ile1124=
ENST00000679858.1:c.*3105C>T	ENSP00000505655.1:n.*3105C>T
ENST00000680211.1:c.324C>T	ENSP00000506102.1:p.Ile108=
ENST00000680280.1:n.1226C>T
ENST00000680349.1:n.2372C>T
ENST00000680403.1:c.3708C>T	ENSP00000505677.1:p.Ile1236=
ENST00000680564.1:c.3474C>T	ENSP00000505582.1:p.Ile1158=
ENST00000680590.1:c.*2103C>T	ENSP00000505350.1:n.*2103C>T
ENST00000680597.1:c.456C>T
ENST00000680739.1:c.738C>T
ENST00000680773.1:n.2224C>T
ENST00000680806.1:c.*3026C>T	ENSP00000506418.1:n.*3026C>T
ENST00000680997.1:n.1655C>T
ENST00000681608.1:n.1568C>T
ENST00000681625.1:c.*1055C>T	ENSP00000505555.1:n.*1055C>T
ENST00000681648.1:n.1238C>T
ENST00000270301.11:c.3708C>T	ENSP00000270301.6:p.Ile1236=
ENST00000401500.6:c.3723C>T	ENSP00000384792.1:p.Ile1241=
ENST00000587391.5:c.*3583C>T	ENSP00000465525.1:n.*3583C>T
NM_001083961.1:c.3723C>T	NP_001077430.1:p.Ile1241=
NM_173636.4:c.3708C>T	NP_775907.4:p.Ile1236=
XM_005258809.2:c.3612C>T	XP_005258866.1:p.Ile1204=
XM_011526837.1:c.3708C>T	XP_011525139.1:p.Ile1236=
XM_011526838.1:c.3474C>T	XP_011525140.1:p.Ile1158=
XM_011526839.1:c.3372C>T	XP_011525141.1:p.Ile1124=
XM_011526840.1:c.2715C>T	XP_011525142.1:p.Ile905=
XM_011526841.1:c.2301C>T	XP_011525143.1:p.Ile767=
XM_011526842.1:c.2154C>T	XP_011525144.1:p.Ile718=
XM_011526843.1:c.1470C>T	XP_011525145.1:p.Ile490=
XM_011526844.1:c.1470C>T	XP_011525146.1:p.Ile490=
XM_011526840.2:c.2715C>T	XP_011525142.1:p.Ile905=
XM_011526841.2:c.2301C>T	XP_011525143.1:p.Ile767=
XM_011526844.2:c.1470C>T	XP_011525146.1:p.Ile490=
XM_017026665.1:c.3723C>T	XP_016882154.1:p.Ile1241=
NM_001083961.2:c.3723C>T MANE Select	NP_001077430.1:p.Ile1241=
NM_173636.5:c.3708C>T	NP_775907.4:p.Ile1236=