Canonical Allele Identifier: CA356637473

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245977G>C (hg19) ; chr4:g.39244357G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244357G>C , CM000666.2:g.39244357G>C	GRCh38
NC_000004.11:g.39245977G>C , CM000666.1:g.39245977G>C	GRCh37
NC_000004.10:g.38922372G>C	NCBI36
NG_031813.1:g.66954G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2531G>C MANE Select	ENSP00000382717.3:p.Arg844Thr
ENST00000399820.7:c.2531G>C	ENSP00000382717.3:p.Arg844Thr
ENST00000506869.5:c.*2112G>C	ENSP00000424319.1:n.*2112G>C
ENST00000512095.5:n.1529G>C
NM_025132.3:c.2531G>C	NP_079408.3:p.Arg844Thr
XM_011513724.1:c.2543G>C	XP_011512026.1:p.Arg848Thr
XM_011513725.1:c.2477G>C	XP_011512027.1:p.Arg826Thr
XM_011513726.1:c.2063G>C	XP_011512028.1:p.Arg688Thr
XM_011513727.1:c.2063G>C	XP_011512029.1:p.Arg688Thr
XM_011513728.1:c.2051G>C	XP_011512030.1:p.Arg684Thr
XM_011513729.1:c.2543G>C	XP_011512031.1:p.Arg848Thr
XR_925155.1:n.2607G>C
NM_001317924.1:c.2051G>C	NP_001304853.1:p.Arg684Thr
XM_011513725.2:c.2477G>C	XP_011512027.1:p.Arg826Thr
XM_011513726.3:c.2063G>C	XP_011512028.1:p.Arg688Thr
XM_017008501.1:c.2051G>C	XP_016863990.1:p.Arg684Thr
XR_001741306.1:n.2607G>C
XR_001741307.1:n.2595G>C
XR_001741308.1:n.2607G>C
XR_001741309.1:n.2595G>C
XR_001741310.1:n.2595G>C
XR_001741311.2:n.2444G>C
NM_025132.4:c.2531G>C MANE Select	NP_079408.3:p.Arg844Thr
NM_001317924.2:c.2051G>C	NP_001304853.1:p.Arg684Thr