Canonical Allele Identifier: CA405450444

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102091-C-T
• COSMIC: COSM1494301
• MyVariant Identifiers: chr19:g.36592993C>T (hg19) ; chr19:g.36102091C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102091C>T , CM000681.2:g.36102091C>T	GRCh38
NC_000019.9:g.36592993C>T , CM000681.1:g.36592993C>T	GRCh37
NC_000019.8:g.41284833C>T	NCBI36
NG_028101.1:g.52211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3160C>T	ENSP00000270301.6:p.Pro1054Ser
ENST00000401500.7:c.3160C>T MANE Select	ENSP00000384792.1:p.Pro1054Ser
ENST00000587391.6:c.*2435C>T	ENSP00000465525.1:n.*2435C>T
ENST00000679357.1:c.950C>T
ENST00000679422.1:c.839C>T
ENST00000679682.1:c.3145C>T	ENSP00000506226.1:p.Pro1049Ser
ENST00000679714.1:c.3154C>T	ENSP00000506627.1:p.Pro1052Ser
ENST00000679757.1:c.2809C>T	ENSP00000505158.1:p.Pro937Ser
ENST00000679858.1:c.*2542C>T	ENSP00000505655.1:n.*2542C>T
ENST00000680211.1:c.-240C>T	ENSP00000506102.1:n.-240C>T
ENST00000680349.1:n.1143C>T
ENST00000680403.1:c.3160C>T	ENSP00000505677.1:p.Pro1054Ser
ENST00000680564.1:c.2972-646C>T	ENSP00000505582.1:n.2972-646C>T
ENST00000680590.1:c.*1555C>T	ENSP00000505350.1:n.*1555C>T
ENST00000680739.1:c.78C>T
ENST00000680773.1:n.1076C>T
ENST00000680806.1:c.*1878C>T	ENSP00000506418.1:n.*1878C>T
ENST00000680997.1:n.507C>T
ENST00000681088.1:c.822C>T
ENST00000681608.1:n.108C>T
ENST00000681625.1:c.*492C>T	ENSP00000505555.1:n.*492C>T
ENST00000270301.11:c.3160C>T	ENSP00000270301.6:p.Pro1054Ser
ENST00000401500.6:c.3160C>T	ENSP00000384792.1:p.Pro1054Ser
ENST00000587391.5:c.*2435C>T	ENSP00000465525.1:n.*2435C>T
NM_001083961.1:c.3160C>T	NP_001077430.1:p.Pro1054Ser
NM_173636.4:c.3160C>T	NP_775907.4:p.Pro1054Ser
XM_005258809.2:c.3049C>T	XP_005258866.1:p.Pro1017Ser
XM_011526837.1:c.3145C>T	XP_011525139.1:p.Pro1049Ser
XM_011526838.1:c.2972-646C>T	XP_011525140.1:n.2972-646C>T
XM_011526839.1:c.2809C>T	XP_011525141.1:p.Pro937Ser
XM_011526840.1:c.2152C>T	XP_011525142.1:p.Pro718Ser
XM_011526841.1:c.1738C>T	XP_011525143.1:p.Pro580Ser
XM_011526842.1:c.1591C>T	XP_011525144.1:p.Pro531Ser
XM_011526843.1:c.907C>T	XP_011525145.1:p.Pro303Ser
XM_011526844.1:c.907C>T	XP_011525146.1:p.Pro303Ser
XM_011526840.2:c.2152C>T	XP_011525142.1:p.Pro718Ser
XM_011526841.2:c.1738C>T	XP_011525143.1:p.Pro580Ser
XM_011526844.2:c.907C>T	XP_011525146.1:p.Pro303Ser
XM_017026665.1:c.3160C>T	XP_016882154.1:p.Pro1054Ser
NM_001083961.2:c.3160C>T MANE Select	NP_001077430.1:p.Pro1054Ser
NM_173636.5:c.3160C>T	NP_775907.4:p.Pro1054Ser