Canonical Allele Identifier: CA356634349

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207245A>C (hg19) ; chr4:g.39205625A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205625A>C , CM000666.2:g.39205625A>C	GRCh38
NC_000004.11:g.39207245A>C , CM000666.1:g.39207245A>C	GRCh37
NC_000004.10:g.38883640A>C	NCBI36
NG_031813.1:g.28222A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.779A>C MANE Select	ENSP00000382717.3:p.His260Pro
ENST00000399820.7:c.779A>C	ENSP00000382717.3:p.His260Pro
ENST00000503697.5:c.*247A>C	ENSP00000423706.1:n.*247A>C
ENST00000506503.1:c.779A>C	ENSP00000423491.1:p.His260Pro
ENST00000506869.5:c.*360A>C	ENSP00000424319.1:n.*360A>C
ENST00000511729.5:n.41-22933A>C
ENST00000512448.1:n.373A>C
NM_025132.3:c.779A>C	NP_079408.3:p.His260Pro
XM_011513724.1:c.779A>C	XP_011512026.1:p.His260Pro
XM_011513725.1:c.713A>C	XP_011512027.1:p.His238Pro
XM_011513726.1:c.299A>C	XP_011512028.1:p.His100Pro
XM_011513727.1:c.299A>C	XP_011512029.1:p.His100Pro
XM_011513728.1:c.299A>C	XP_011512030.1:p.His100Pro
XM_011513729.1:c.779A>C	XP_011512031.1:p.His260Pro
XR_925155.1:n.843A>C
NM_001317924.1:c.299A>C	NP_001304853.1:p.His100Pro
XM_011513725.2:c.713A>C	XP_011512027.1:p.His238Pro
XM_011513726.3:c.299A>C	XP_011512028.1:p.His100Pro
XM_017008501.1:c.299A>C	XP_016863990.1:p.His100Pro
XR_001741306.1:n.843A>C
XR_001741307.1:n.843A>C
XR_001741308.1:n.843A>C
XR_001741309.1:n.843A>C
XR_001741310.1:n.843A>C
XR_001741311.2:n.692A>C
XR_001741312.1:n.843A>C
NM_025132.4:c.779A>C MANE Select	NP_079408.3:p.His260Pro
NM_001317924.2:c.299A>C	NP_001304853.1:p.His100Pro