Canonical Allele Identifier: CA438943913

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278730A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277110A>C , CM000666.2:g.39277110A>C	GRCh38
NC_000004.11:g.39278730A>C , CM000666.1:g.39278730A>C	GRCh37
NC_000004.10:g.38955125A>C	NCBI36
NG_031813.1:g.99707A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3807A>C MANE Select	ENSP00000382717.3:p.Gly1269=
ENST00000399820.7:c.3807A>C	ENSP00000382717.3:p.Gly1269=
ENST00000503733.1:n.147A>C
ENST00000506869.5:c.*3388A>C	ENSP00000424319.1:n.*3388A>C
ENST00000512534.5:n.2118A>C
ENST00000512588.5:n.149A>C
NM_025132.3:c.3807A>C	NP_079408.3:p.Gly1269=
XM_011513724.1:c.3819A>C	XP_011512026.1:p.Gly1273=
XM_011513725.1:c.3753A>C	XP_011512027.1:p.Gly1251=
XM_011513726.1:c.3339A>C	XP_011512028.1:p.Gly1113=
XM_011513727.1:c.3339A>C	XP_011512029.1:p.Gly1113=
XM_011513728.1:c.3327A>C	XP_011512030.1:p.Gly1109=
XR_925155.1:n.5517A>C
NM_001317924.1:c.3327A>C	NP_001304853.1:p.Gly1109=
XM_011513725.2:c.3753A>C	XP_011512027.1:p.Gly1251=
XM_011513726.3:c.3339A>C	XP_011512028.1:p.Gly1113=
XM_017008501.1:c.3327A>C	XP_016863990.1:p.Gly1109=
XR_001741306.1:n.4084A>C
XR_001741307.1:n.4072A>C
XR_001741308.1:n.5718A>C
XR_001741309.1:n.5505A>C
XR_001741310.1:n.5706A>C
XR_001741311.2:n.5354A>C
NM_025132.4:c.3807A>C MANE Select	NP_079408.3:p.Gly1269=
NM_001317924.2:c.3327A>C	NP_001304853.1:p.Gly1109=