Canonical Allele Identifier: CA438942000

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245897G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244277G>T , CM000666.2:g.39244277G>T	GRCh38
NC_000004.11:g.39245897G>T , CM000666.1:g.39245897G>T	GRCh37
NC_000004.10:g.38922292G>T	NCBI36
NG_031813.1:g.66874G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2451G>T MANE Select	ENSP00000382717.3:p.Val817=
ENST00000399820.7:c.2451G>T	ENSP00000382717.3:p.Val817=
ENST00000506869.5:c.*2032G>T	ENSP00000424319.1:n.*2032G>T
ENST00000512095.5:n.1449G>T
NM_025132.3:c.2451G>T	NP_079408.3:p.Val817=
XM_011513724.1:c.2463G>T	XP_011512026.1:p.Val821=
XM_011513725.1:c.2397G>T	XP_011512027.1:p.Val799=
XM_011513726.1:c.1983G>T	XP_011512028.1:p.Val661=
XM_011513727.1:c.1983G>T	XP_011512029.1:p.Val661=
XM_011513728.1:c.1971G>T	XP_011512030.1:p.Val657=
XM_011513729.1:c.2463G>T	XP_011512031.1:p.Val821=
XR_925155.1:n.2527G>T
NM_001317924.1:c.1971G>T	NP_001304853.1:p.Val657=
XM_011513725.2:c.2397G>T	XP_011512027.1:p.Val799=
XM_011513726.3:c.1983G>T	XP_011512028.1:p.Val661=
XM_017008501.1:c.1971G>T	XP_016863990.1:p.Val657=
XR_001741306.1:n.2527G>T
XR_001741307.1:n.2515G>T
XR_001741308.1:n.2527G>T
XR_001741309.1:n.2515G>T
XR_001741310.1:n.2515G>T
XR_001741311.2:n.2364G>T
NM_025132.4:c.2451G>T MANE Select	NP_079408.3:p.Val817=
NM_001317924.2:c.1971G>T	NP_001304853.1:p.Val657=