Canonical Allele Identifier: CA405449452

Gene: WDR62

Linked Data

• gnomAD v4: 19-36101736-C-T
• MyVariant Identifiers: chr19:g.36592638C>T (hg19) ; chr19:g.36101736C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101736C>T , CM000681.2:g.36101736C>T	GRCh38
NC_000019.9:g.36592638C>T , CM000681.1:g.36592638C>T	GRCh37
NC_000019.8:g.41284478C>T	NCBI36
NG_028101.1:g.51856C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3044C>T	ENSP00000270301.6:p.Pro1015Leu
ENST00000401500.7:c.3044C>T MANE Select	ENSP00000384792.1:p.Pro1015Leu
ENST00000587391.6:c.*2080C>T	ENSP00000465525.1:n.*2080C>T
ENST00000679357.1:c.834C>T
ENST00000679422.1:c.762-278C>T
ENST00000679682.1:c.3029C>T	ENSP00000506226.1:p.Pro1010Leu
ENST00000679714.1:c.3038C>T	ENSP00000506627.1:p.Pro1013Leu
ENST00000679757.1:c.2693C>T	ENSP00000505158.1:p.Pro898Leu
ENST00000679858.1:c.*2187C>T	ENSP00000505655.1:n.*2187C>T
ENST00000680211.1:c.-356C>T	ENSP00000506102.1:n.-356C>T
ENST00000680349.1:n.1027C>T
ENST00000680403.1:c.3044C>T	ENSP00000505677.1:p.Pro1015Leu
ENST00000680564.1:c.2971+419C>T	ENSP00000505582.1:n.2971+419C>T
ENST00000680590.1:c.*1439C>T	ENSP00000505350.1:n.*1439C>T
ENST00000680773.1:n.721C>T
ENST00000680806.1:c.*1801-278C>T	ENSP00000506418.1:n.*1801-278C>T
ENST00000680997.1:n.391C>T
ENST00000681088.1:c.706C>T
ENST00000681625.1:c.*376C>T	ENSP00000505555.1:n.*376C>T
ENST00000270301.11:c.3044C>T	ENSP00000270301.6:p.Pro1015Leu
ENST00000401500.6:c.3044C>T	ENSP00000384792.1:p.Pro1015Leu
ENST00000587391.5:c.*2080C>T	ENSP00000465525.1:n.*2080C>T
NM_001083961.1:c.3044C>T	NP_001077430.1:p.Pro1015Leu
NM_173636.4:c.3044C>T	NP_775907.4:p.Pro1015Leu
XM_005258809.2:c.2972-278C>T	XP_005258866.1:n.2972-278C>T
XM_011526837.1:c.3029C>T	XP_011525139.1:p.Pro1010Leu
XM_011526838.1:c.2971+419C>T	XP_011525140.1:n.2971+419C>T
XM_011526839.1:c.2693C>T	XP_011525141.1:p.Pro898Leu
XM_011526840.1:c.2036C>T	XP_011525142.1:p.Pro679Leu
XM_011526841.1:c.1622C>T	XP_011525143.1:p.Pro541Leu
XM_011526842.1:c.1475C>T	XP_011525144.1:p.Pro492Leu
XM_011526843.1:c.791C>T	XP_011525145.1:p.Pro264Leu
XM_011526844.1:c.791C>T	XP_011525146.1:p.Pro264Leu
XM_011526840.2:c.2036C>T	XP_011525142.1:p.Pro679Leu
XM_011526841.2:c.1622C>T	XP_011525143.1:p.Pro541Leu
XM_011526844.2:c.791C>T	XP_011525146.1:p.Pro264Leu
XM_017026665.1:c.3044C>T	XP_016882154.1:p.Pro1015Leu
NM_001083961.2:c.3044C>T MANE Select	NP_001077430.1:p.Pro1015Leu
NM_173636.5:c.3044C>T	NP_775907.4:p.Pro1015Leu