Canonical Allele Identifier: CA438939410

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207279T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205659T>C , CM000666.2:g.39205659T>C	GRCh38
NC_000004.11:g.39207279T>C , CM000666.1:g.39207279T>C	GRCh37
NC_000004.10:g.38883674T>C	NCBI36
NG_031813.1:g.28256T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.813T>C MANE Select	ENSP00000382717.3:p.Ala271=
ENST00000399820.7:c.813T>C	ENSP00000382717.3:p.Ala271=
ENST00000503697.5:c.*281T>C	ENSP00000423706.1:n.*281T>C
ENST00000506503.1:c.813T>C	ENSP00000423491.1:p.Ala271=
ENST00000506869.5:c.*394T>C	ENSP00000424319.1:n.*394T>C
ENST00000511729.5:n.41-22899T>C
ENST00000512448.1:n.407T>C
NM_025132.3:c.813T>C	NP_079408.3:p.Ala271=
XM_011513724.1:c.813T>C	XP_011512026.1:p.Ala271=
XM_011513725.1:c.747T>C	XP_011512027.1:p.Ala249=
XM_011513726.1:c.333T>C	XP_011512028.1:p.Ala111=
XM_011513727.1:c.333T>C	XP_011512029.1:p.Ala111=
XM_011513728.1:c.333T>C	XP_011512030.1:p.Ala111=
XM_011513729.1:c.813T>C	XP_011512031.1:p.Ala271=
XR_925155.1:n.877T>C
NM_001317924.1:c.333T>C	NP_001304853.1:p.Ala111=
XM_011513725.2:c.747T>C	XP_011512027.1:p.Ala249=
XM_011513726.3:c.333T>C	XP_011512028.1:p.Ala111=
XM_017008501.1:c.333T>C	XP_016863990.1:p.Ala111=
XR_001741306.1:n.877T>C
XR_001741307.1:n.877T>C
XR_001741308.1:n.877T>C
XR_001741309.1:n.877T>C
XR_001741310.1:n.877T>C
XR_001741311.2:n.726T>C
XR_001741312.1:n.877T>C
NM_025132.4:c.813T>C MANE Select	NP_079408.3:p.Ala271=
NM_001317924.2:c.333T>C	NP_001304853.1:p.Ala111=