Canonical Allele Identifier: CA405451444

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593656C>A (hg19) ; chr19:g.36102754C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102754C>A , CM000681.2:g.36102754C>A	GRCh38
NC_000019.9:g.36593656C>A , CM000681.1:g.36593656C>A	GRCh37
NC_000019.8:g.41285496C>A	NCBI36
NG_028101.1:g.52874C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3223C>A	ENSP00000270301.6:p.Leu1075Met
ENST00000401500.7:c.3238C>A MANE Select	ENSP00000384792.1:p.Leu1080Met
ENST00000587391.6:c.*3098C>A	ENSP00000465525.1:n.*3098C>A
ENST00000679357.1:c.1318C>A
ENST00000679598.1:c.3C>A
ENST00000679682.1:c.3223C>A	ENSP00000506226.1:p.Leu1075Met
ENST00000679714.1:c.3232C>A	ENSP00000506627.1:p.Leu1078Met
ENST00000679757.1:c.2887C>A	ENSP00000505158.1:p.Leu963Met
ENST00000679858.1:c.*2620C>A	ENSP00000505655.1:n.*2620C>A
ENST00000680211.1:c.-162C>A	ENSP00000506102.1:n.-162C>A
ENST00000680280.1:n.525C>A
ENST00000680349.1:n.1806C>A
ENST00000680403.1:c.3223C>A	ENSP00000505677.1:p.Leu1075Met
ENST00000680564.1:c.2989C>A	ENSP00000505582.1:p.Leu997Met
ENST00000680590.1:c.*1618C>A	ENSP00000505350.1:n.*1618C>A
ENST00000680597.1:c.3C>A
ENST00000680739.1:c.253C>A
ENST00000680773.1:n.1739C>A
ENST00000680806.1:c.*2541C>A	ENSP00000506418.1:n.*2541C>A
ENST00000680997.1:n.1170C>A
ENST00000681608.1:n.771C>A
ENST00000681625.1:c.*570C>A	ENSP00000505555.1:n.*570C>A
ENST00000681648.1:n.537C>A
ENST00000270301.11:c.3223C>A	ENSP00000270301.6:p.Leu1075Met
ENST00000401500.6:c.3238C>A	ENSP00000384792.1:p.Leu1080Met
ENST00000587391.5:c.*3098C>A	ENSP00000465525.1:n.*3098C>A
NM_001083961.1:c.3238C>A	NP_001077430.1:p.Leu1080Met
NM_173636.4:c.3223C>A	NP_775907.4:p.Leu1075Met
XM_005258809.2:c.3127C>A	XP_005258866.1:p.Leu1043Met
XM_011526837.1:c.3223C>A	XP_011525139.1:p.Leu1075Met
XM_011526838.1:c.2989C>A	XP_011525140.1:p.Leu997Met
XM_011526839.1:c.2887C>A	XP_011525141.1:p.Leu963Met
XM_011526840.1:c.2230C>A	XP_011525142.1:p.Leu744Met
XM_011526841.1:c.1816C>A	XP_011525143.1:p.Leu606Met
XM_011526842.1:c.1669C>A	XP_011525144.1:p.Leu557Met
XM_011526843.1:c.985C>A	XP_011525145.1:p.Leu329Met
XM_011526844.1:c.985C>A	XP_011525146.1:p.Leu329Met
XM_011526840.2:c.2230C>A	XP_011525142.1:p.Leu744Met
XM_011526841.2:c.1816C>A	XP_011525143.1:p.Leu606Met
XM_011526844.2:c.985C>A	XP_011525146.1:p.Leu329Met
XM_017026665.1:c.3238C>A	XP_016882154.1:p.Leu1080Met
NM_001083961.2:c.3238C>A MANE Select	NP_001077430.1:p.Leu1080Met
NM_173636.5:c.3223C>A	NP_775907.4:p.Leu1075Met