Canonical Allele Identifier: CA356634267

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207206T>C (hg19) ; chr4:g.39205586T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205586T>C , CM000666.2:g.39205586T>C	GRCh38
NC_000004.11:g.39207206T>C , CM000666.1:g.39207206T>C	GRCh37
NC_000004.10:g.38883601T>C	NCBI36
NG_031813.1:g.28183T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.740T>C MANE Select	ENSP00000382717.3:p.Ile247Thr
ENST00000399820.7:c.740T>C	ENSP00000382717.3:p.Ile247Thr
ENST00000503697.5:c.*208T>C	ENSP00000423706.1:n.*208T>C
ENST00000506503.1:c.740T>C	ENSP00000423491.1:p.Ile247Thr
ENST00000506869.5:c.*321T>C	ENSP00000424319.1:n.*321T>C
ENST00000511729.5:n.41-22972T>C
ENST00000512448.1:n.334T>C
NM_025132.3:c.740T>C	NP_079408.3:p.Ile247Thr
XM_011513724.1:c.740T>C	XP_011512026.1:p.Ile247Thr
XM_011513725.1:c.674T>C	XP_011512027.1:p.Ile225Thr
XM_011513726.1:c.260T>C	XP_011512028.1:p.Ile87Thr
XM_011513727.1:c.260T>C	XP_011512029.1:p.Ile87Thr
XM_011513728.1:c.260T>C	XP_011512030.1:p.Ile87Thr
XM_011513729.1:c.740T>C	XP_011512031.1:p.Ile247Thr
XR_925155.1:n.804T>C
NM_001317924.1:c.260T>C	NP_001304853.1:p.Ile87Thr
XM_011513725.2:c.674T>C	XP_011512027.1:p.Ile225Thr
XM_011513726.3:c.260T>C	XP_011512028.1:p.Ile87Thr
XM_017008501.1:c.260T>C	XP_016863990.1:p.Ile87Thr
XR_001741306.1:n.804T>C
XR_001741307.1:n.804T>C
XR_001741308.1:n.804T>C
XR_001741309.1:n.804T>C
XR_001741310.1:n.804T>C
XR_001741311.2:n.653T>C
XR_001741312.1:n.804T>C
NM_025132.4:c.740T>C MANE Select	NP_079408.3:p.Ile247Thr
NM_001317924.2:c.260T>C	NP_001304853.1:p.Ile87Thr