Canonical Allele Identifier: CA356634590

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207355T>C (hg19) ; chr4:g.39205735T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205735T>C , CM000666.2:g.39205735T>C	GRCh38
NC_000004.11:g.39207355T>C , CM000666.1:g.39207355T>C	GRCh37
NC_000004.10:g.38883750T>C	NCBI36
NG_031813.1:g.28332T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.889T>C MANE Select	ENSP00000382717.3:p.Cys297Arg
ENST00000399820.7:c.889T>C	ENSP00000382717.3:p.Cys297Arg
ENST00000503697.5:c.*357T>C	ENSP00000423706.1:n.*357T>C
ENST00000506503.1:c.889T>C	ENSP00000423491.1:p.Cys297Arg
ENST00000506869.5:c.*470T>C	ENSP00000424319.1:n.*470T>C
ENST00000511729.5:n.41-22823T>C
ENST00000512448.1:n.483T>C
NM_025132.3:c.889T>C	NP_079408.3:p.Cys297Arg
XM_011513724.1:c.889T>C	XP_011512026.1:p.Cys297Arg
XM_011513725.1:c.823T>C	XP_011512027.1:p.Cys275Arg
XM_011513726.1:c.409T>C	XP_011512028.1:p.Cys137Arg
XM_011513727.1:c.409T>C	XP_011512029.1:p.Cys137Arg
XM_011513728.1:c.409T>C	XP_011512030.1:p.Cys137Arg
XM_011513729.1:c.889T>C	XP_011512031.1:p.Cys297Arg
XR_925155.1:n.953T>C
NM_001317924.1:c.409T>C	NP_001304853.1:p.Cys137Arg
XM_011513725.2:c.823T>C	XP_011512027.1:p.Cys275Arg
XM_011513726.3:c.409T>C	XP_011512028.1:p.Cys137Arg
XM_017008501.1:c.409T>C	XP_016863990.1:p.Cys137Arg
XR_001741306.1:n.953T>C
XR_001741307.1:n.953T>C
XR_001741308.1:n.953T>C
XR_001741309.1:n.953T>C
XR_001741310.1:n.953T>C
XR_001741311.2:n.802T>C
XR_001741312.1:n.953T>C
NM_025132.4:c.889T>C MANE Select	NP_079408.3:p.Cys297Arg
NM_001317924.2:c.409T>C	NP_001304853.1:p.Cys137Arg