Canonical Allele Identifier: CA356647290

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39274630G>C (hg19) ; chr4:g.39273010G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273010G>C , CM000666.2:g.39273010G>C	GRCh38
NC_000004.11:g.39274630G>C , CM000666.1:g.39274630G>C	GRCh37
NC_000004.10:g.38951025G>C	NCBI36
NG_031813.1:g.95607G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3514G>C MANE Select	ENSP00000382717.3:p.Gly1172Arg
ENST00000399820.7:c.3514G>C	ENSP00000382717.3:p.Gly1172Arg
ENST00000506869.5:c.*3095G>C	ENSP00000424319.1:n.*3095G>C
ENST00000512095.5:n.2512G>C
ENST00000512534.5:n.79G>C
NM_025132.3:c.3514G>C	NP_079408.3:p.Gly1172Arg
XM_011513724.1:c.3526G>C	XP_011512026.1:p.Gly1176Arg
XM_011513725.1:c.3460G>C	XP_011512027.1:p.Gly1154Arg
XM_011513726.1:c.3046G>C	XP_011512028.1:p.Gly1016Arg
XM_011513727.1:c.3046G>C	XP_011512029.1:p.Gly1016Arg
XM_011513728.1:c.3034G>C	XP_011512030.1:p.Gly1012Arg
XR_925155.1:n.3590G>C
NM_001317924.1:c.3034G>C	NP_001304853.1:p.Gly1012Arg
XM_011513725.2:c.3460G>C	XP_011512027.1:p.Gly1154Arg
XM_011513726.3:c.3046G>C	XP_011512028.1:p.Gly1016Arg
XM_017008501.1:c.3034G>C	XP_016863990.1:p.Gly1012Arg
XR_001741306.1:n.3590G>C
XR_001741307.1:n.3578G>C
XR_001741308.1:n.3590G>C
XR_001741309.1:n.3578G>C
XR_001741310.1:n.3578G>C
XR_001741311.2:n.3427G>C
NM_025132.4:c.3514G>C MANE Select	NP_079408.3:p.Gly1172Arg
NM_001317924.2:c.3034G>C	NP_001304853.1:p.Gly1012Arg