Canonical Allele Identifier: CA356637530

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246003A>G (hg19) ; chr4:g.39244383A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244383A>G , CM000666.2:g.39244383A>G	GRCh38
NC_000004.11:g.39246003A>G , CM000666.1:g.39246003A>G	GRCh37
NC_000004.10:g.38922398A>G	NCBI36
NG_031813.1:g.66980A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2557A>G MANE Select	ENSP00000382717.3:p.Met853Val
ENST00000399820.7:c.2557A>G	ENSP00000382717.3:p.Met853Val
ENST00000506869.5:c.*2138A>G	ENSP00000424319.1:n.*2138A>G
ENST00000512095.5:n.1555A>G
NM_025132.3:c.2557A>G	NP_079408.3:p.Met853Val
XM_011513724.1:c.2569A>G	XP_011512026.1:p.Met857Val
XM_011513725.1:c.2503A>G	XP_011512027.1:p.Met835Val
XM_011513726.1:c.2089A>G	XP_011512028.1:p.Met697Val
XM_011513727.1:c.2089A>G	XP_011512029.1:p.Met697Val
XM_011513728.1:c.2077A>G	XP_011512030.1:p.Met693Val
XM_011513729.1:c.2569A>G	XP_011512031.1:p.Met857Val
XR_925155.1:n.2633A>G
NM_001317924.1:c.2077A>G	NP_001304853.1:p.Met693Val
XM_011513725.2:c.2503A>G	XP_011512027.1:p.Met835Val
XM_011513726.3:c.2089A>G	XP_011512028.1:p.Met697Val
XM_017008501.1:c.2077A>G	XP_016863990.1:p.Met693Val
XR_001741306.1:n.2633A>G
XR_001741307.1:n.2621A>G
XR_001741308.1:n.2633A>G
XR_001741309.1:n.2621A>G
XR_001741310.1:n.2621A>G
XR_001741311.2:n.2470A>G
NM_025132.4:c.2557A>G MANE Select	NP_079408.3:p.Met853Val
NM_001317924.2:c.2077A>G	NP_001304853.1:p.Met693Val