Canonical Allele Identifier: CA356638342

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246105G>C (hg19) ; chr4:g.39244485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244485G>C , CM000666.2:g.39244485G>C	GRCh38
NC_000004.11:g.39246105G>C , CM000666.1:g.39246105G>C	GRCh37
NC_000004.10:g.38922500G>C	NCBI36
NG_031813.1:g.67082G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2578G>C MANE Select	ENSP00000382717.3:p.Ala860Pro
ENST00000399820.7:c.2578G>C	ENSP00000382717.3:p.Ala860Pro
ENST00000506869.5:c.*2159G>C	ENSP00000424319.1:n.*2159G>C
ENST00000512095.5:n.1576G>C
NM_025132.3:c.2578G>C	NP_079408.3:p.Ala860Pro
XM_011513724.1:c.2590G>C	XP_011512026.1:p.Ala864Pro
XM_011513725.1:c.2524G>C	XP_011512027.1:p.Ala842Pro
XM_011513726.1:c.2110G>C	XP_011512028.1:p.Ala704Pro
XM_011513727.1:c.2110G>C	XP_011512029.1:p.Ala704Pro
XM_011513728.1:c.2098G>C	XP_011512030.1:p.Ala700Pro
XM_011513729.1:c.2590G>C	XP_011512031.1:p.Ala864Pro
XR_925155.1:n.2654G>C
NM_001317924.1:c.2098G>C	NP_001304853.1:p.Ala700Pro
XM_011513725.2:c.2524G>C	XP_011512027.1:p.Ala842Pro
XM_011513726.3:c.2110G>C	XP_011512028.1:p.Ala704Pro
XM_017008501.1:c.2098G>C	XP_016863990.1:p.Ala700Pro
XR_001741306.1:n.2654G>C
XR_001741307.1:n.2642G>C
XR_001741308.1:n.2654G>C
XR_001741309.1:n.2642G>C
XR_001741310.1:n.2642G>C
XR_001741311.2:n.2491G>C
NM_025132.4:c.2578G>C MANE Select	NP_079408.3:p.Ala860Pro
NM_001317924.2:c.2098G>C	NP_001304853.1:p.Ala700Pro