Canonical Allele Identifier: CA356647585

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274675C>G (hg19) ; chr4:g.39273055C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273055C>G , CM000666.2:g.39273055C>G	GRCh38
NC_000004.11:g.39274675C>G , CM000666.1:g.39274675C>G	GRCh37
NC_000004.10:g.38951070C>G	NCBI36
NG_031813.1:g.95652C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3559C>G MANE Select	ENSP00000382717.3:p.Pro1187Ala
ENST00000399820.7:c.3559C>G	ENSP00000382717.3:p.Pro1187Ala
ENST00000506869.5:c.*3140C>G	ENSP00000424319.1:n.*3140C>G
ENST00000512095.5:n.2557C>G
ENST00000512534.5:n.124C>G
NM_025132.3:c.3559C>G	NP_079408.3:p.Pro1187Ala
XM_011513724.1:c.3571C>G	XP_011512026.1:p.Pro1191Ala
XM_011513725.1:c.3505C>G	XP_011512027.1:p.Pro1169Ala
XM_011513726.1:c.3091C>G	XP_011512028.1:p.Pro1031Ala
XM_011513727.1:c.3091C>G	XP_011512029.1:p.Pro1031Ala
XM_011513728.1:c.3079C>G	XP_011512030.1:p.Pro1027Ala
XR_925155.1:n.3635C>G
NM_001317924.1:c.3079C>G	NP_001304853.1:p.Pro1027Ala
XM_011513725.2:c.3505C>G	XP_011512027.1:p.Pro1169Ala
XM_011513726.3:c.3091C>G	XP_011512028.1:p.Pro1031Ala
XM_017008501.1:c.3079C>G	XP_016863990.1:p.Pro1027Ala
XR_001741306.1:n.3635C>G
XR_001741307.1:n.3623C>G
XR_001741308.1:n.3635C>G
XR_001741309.1:n.3623C>G
XR_001741310.1:n.3623C>G
XR_001741311.2:n.3472C>G
NM_025132.4:c.3559C>G MANE Select	NP_079408.3:p.Pro1187Ala
NM_001317924.2:c.3079C>G	NP_001304853.1:p.Pro1027Ala