Canonical Allele Identifier: CA356650932

Gene: WDR19

Linked Data

• gnomAD v4: 4-39274953-G-A
• MyVariant Identifiers: chr4:g.39276573G>A (hg19) ; chr4:g.39274953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274953G>A , CM000666.2:g.39274953G>A	GRCh38
NC_000004.11:g.39276573G>A , CM000666.1:g.39276573G>A	GRCh37
NC_000004.10:g.38952968G>A	NCBI36
NG_031813.1:g.97550G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3711G>A MANE Select	ENSP00000382717.3:p.Met1237Ile
ENST00000399820.7:c.3711G>A	ENSP00000382717.3:p.Met1237Ile
ENST00000506869.5:c.*3292G>A	ENSP00000424319.1:n.*3292G>A
ENST00000512095.5:n.2709G>A
ENST00000512534.5:n.2022G>A
NM_025132.3:c.3711G>A	NP_079408.3:p.Met1237Ile
XM_011513724.1:c.3723G>A	XP_011512026.1:p.Met1241Ile
XM_011513725.1:c.3657G>A	XP_011512027.1:p.Met1219Ile
XM_011513726.1:c.3243G>A	XP_011512028.1:p.Met1081Ile
XM_011513727.1:c.3243G>A	XP_011512029.1:p.Met1081Ile
XM_011513728.1:c.3231G>A	XP_011512030.1:p.Met1077Ile
XR_925155.1:n.5421G>A
NM_001317924.1:c.3231G>A	NP_001304853.1:p.Met1077Ile
XM_011513725.2:c.3657G>A	XP_011512027.1:p.Met1219Ile
XM_011513726.3:c.3243G>A	XP_011512028.1:p.Met1081Ile
XM_017008501.1:c.3231G>A	XP_016863990.1:p.Met1077Ile
XR_001741306.1:n.3787G>A
XR_001741307.1:n.3775G>A
XR_001741308.1:n.5421G>A
XR_001741309.1:n.5409G>A
XR_001741310.1:n.5409G>A
XR_001741311.2:n.5258G>A
NM_025132.4:c.3711G>A MANE Select	NP_079408.3:p.Met1237Ile
NM_001317924.2:c.3231G>A	NP_001304853.1:p.Met1077Ile