Canonical Allele Identifier: CA405450109

Gene: WDR62

Linked Data

• dbSNP Id: rs1259527640
• gnomAD v2: 19-36592952-C-T
• gnomAD v4: 19-36102050-C-T
• MyVariant Identifiers: chr19:g.36592952C>T (hg19) ; chr19:g.36102050C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102050C>T , CM000681.2:g.36102050C>T	GRCh38
NC_000019.9:g.36592952C>T , CM000681.1:g.36592952C>T	GRCh37
NC_000019.8:g.41284792C>T	NCBI36
NG_028101.1:g.52170C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3119C>T	ENSP00000270301.6:p.Pro1040Leu
ENST00000401500.7:c.3119C>T MANE Select	ENSP00000384792.1:p.Pro1040Leu
ENST00000587391.6:c.*2394C>T	ENSP00000465525.1:n.*2394C>T
ENST00000679357.1:c.909C>T
ENST00000679422.1:c.798C>T
ENST00000679682.1:c.3104C>T	ENSP00000506226.1:p.Pro1035Leu
ENST00000679714.1:c.3113C>T	ENSP00000506627.1:p.Pro1038Leu
ENST00000679757.1:c.2768C>T	ENSP00000505158.1:p.Pro923Leu
ENST00000679858.1:c.*2501C>T	ENSP00000505655.1:n.*2501C>T
ENST00000680211.1:c.-281C>T	ENSP00000506102.1:n.-281C>T
ENST00000680349.1:n.1102C>T
ENST00000680403.1:c.3119C>T	ENSP00000505677.1:p.Pro1040Leu
ENST00000680564.1:c.2972-687C>T	ENSP00000505582.1:n.2972-687C>T
ENST00000680590.1:c.*1514C>T	ENSP00000505350.1:n.*1514C>T
ENST00000680739.1:c.37C>T
ENST00000680773.1:n.1035C>T
ENST00000680806.1:c.*1837C>T	ENSP00000506418.1:n.*1837C>T
ENST00000680997.1:n.466C>T
ENST00000681088.1:c.781C>T
ENST00000681608.1:n.67C>T
ENST00000681625.1:c.*451C>T	ENSP00000505555.1:n.*451C>T
ENST00000270301.11:c.3119C>T	ENSP00000270301.6:p.Pro1040Leu
ENST00000401500.6:c.3119C>T	ENSP00000384792.1:p.Pro1040Leu
ENST00000587391.5:c.*2394C>T	ENSP00000465525.1:n.*2394C>T
NM_001083961.1:c.3119C>T	NP_001077430.1:p.Pro1040Leu
NM_173636.4:c.3119C>T	NP_775907.4:p.Pro1040Leu
XM_005258809.2:c.3008C>T	XP_005258866.1:p.Pro1003Leu
XM_011526837.1:c.3104C>T	XP_011525139.1:p.Pro1035Leu
XM_011526838.1:c.2972-687C>T	XP_011525140.1:n.2972-687C>T
XM_011526839.1:c.2768C>T	XP_011525141.1:p.Pro923Leu
XM_011526840.1:c.2111C>T	XP_011525142.1:p.Pro704Leu
XM_011526841.1:c.1697C>T	XP_011525143.1:p.Pro566Leu
XM_011526842.1:c.1550C>T	XP_011525144.1:p.Pro517Leu
XM_011526843.1:c.866C>T	XP_011525145.1:p.Pro289Leu
XM_011526844.1:c.866C>T	XP_011525146.1:p.Pro289Leu
XM_011526840.2:c.2111C>T	XP_011525142.1:p.Pro704Leu
XM_011526841.2:c.1697C>T	XP_011525143.1:p.Pro566Leu
XM_011526844.2:c.866C>T	XP_011525146.1:p.Pro289Leu
XM_017026665.1:c.3119C>T	XP_016882154.1:p.Pro1040Leu
NM_001083961.2:c.3119C>T MANE Select	NP_001077430.1:p.Pro1040Leu
NM_173636.5:c.3119C>T	NP_775907.4:p.Pro1040Leu