Canonical Allele Identifier: CA356638215

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246092A>C (hg19) ; chr4:g.39244472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244472A>C , CM000666.2:g.39244472A>C	GRCh38
NC_000004.11:g.39246092A>C , CM000666.1:g.39246092A>C	GRCh37
NC_000004.10:g.38922487A>C	NCBI36
NG_031813.1:g.67069A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2565A>C MANE Select	ENSP00000382717.3:p.Gln855His
ENST00000399820.7:c.2565A>C	ENSP00000382717.3:p.Gln855His
ENST00000506869.5:c.*2146A>C	ENSP00000424319.1:n.*2146A>C
ENST00000512095.5:n.1563A>C
NM_025132.3:c.2565A>C	NP_079408.3:p.Gln855His
XM_011513724.1:c.2577A>C	XP_011512026.1:p.Gln859His
XM_011513725.1:c.2511A>C	XP_011512027.1:p.Gln837His
XM_011513726.1:c.2097A>C	XP_011512028.1:p.Gln699His
XM_011513727.1:c.2097A>C	XP_011512029.1:p.Gln699His
XM_011513728.1:c.2085A>C	XP_011512030.1:p.Gln695His
XM_011513729.1:c.2577A>C	XP_011512031.1:p.Gln859His
XR_925155.1:n.2641A>C
NM_001317924.1:c.2085A>C	NP_001304853.1:p.Gln695His
XM_011513725.2:c.2511A>C	XP_011512027.1:p.Gln837His
XM_011513726.3:c.2097A>C	XP_011512028.1:p.Gln699His
XM_017008501.1:c.2085A>C	XP_016863990.1:p.Gln695His
XR_001741306.1:n.2641A>C
XR_001741307.1:n.2629A>C
XR_001741308.1:n.2641A>C
XR_001741309.1:n.2629A>C
XR_001741310.1:n.2629A>C
XR_001741311.2:n.2478A>C
NM_025132.4:c.2565A>C MANE Select	NP_079408.3:p.Gln855His
NM_001317924.2:c.2085A>C	NP_001304853.1:p.Gln695His