Canonical Allele Identifier: CA356637509

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245995T>A (hg19) ; chr4:g.39244375T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244375T>A , CM000666.2:g.39244375T>A	GRCh38
NC_000004.11:g.39245995T>A , CM000666.1:g.39245995T>A	GRCh37
NC_000004.10:g.38922390T>A	NCBI36
NG_031813.1:g.66972T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2549T>A MANE Select	ENSP00000382717.3:p.Leu850Ter
ENST00000399820.7:c.2549T>A	ENSP00000382717.3:p.Leu850Ter
ENST00000506869.5:c.*2130T>A	ENSP00000424319.1:n.*2130T>A
ENST00000512095.5:n.1547T>A
NM_025132.3:c.2549T>A	NP_079408.3:p.Leu850Ter
XM_011513724.1:c.2561T>A	XP_011512026.1:p.Leu854Ter
XM_011513725.1:c.2495T>A	XP_011512027.1:p.Leu832Ter
XM_011513726.1:c.2081T>A	XP_011512028.1:p.Leu694Ter
XM_011513727.1:c.2081T>A	XP_011512029.1:p.Leu694Ter
XM_011513728.1:c.2069T>A	XP_011512030.1:p.Leu690Ter
XM_011513729.1:c.2561T>A	XP_011512031.1:p.Leu854Ter
XR_925155.1:n.2625T>A
NM_001317924.1:c.2069T>A	NP_001304853.1:p.Leu690Ter
XM_011513725.2:c.2495T>A	XP_011512027.1:p.Leu832Ter
XM_011513726.3:c.2081T>A	XP_011512028.1:p.Leu694Ter
XM_017008501.1:c.2069T>A	XP_016863990.1:p.Leu690Ter
XR_001741306.1:n.2625T>A
XR_001741307.1:n.2613T>A
XR_001741308.1:n.2625T>A
XR_001741309.1:n.2613T>A
XR_001741310.1:n.2613T>A
XR_001741311.2:n.2462T>A
NM_025132.4:c.2549T>A MANE Select	NP_079408.3:p.Leu850Ter
NM_001317924.2:c.2069T>A	NP_001304853.1:p.Leu690Ter