Canonical Allele Identifier: CA356646218

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39270014T>C , CM000666.2:g.39270014T>C	GRCh38
NC_000004.11:g.39271634T>C , CM000666.1:g.39271634T>C	GRCh37
NC_000004.10:g.38948029T>C	NCBI36
NG_031813.1:g.92611T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3397T>C MANE Select	ENSP00000382717.3:p.Tyr1133His
ENST00000399820.7:c.3397T>C	ENSP00000382717.3:p.Tyr1133His
ENST00000506869.5:c.*2978T>C	ENSP00000424319.1:n.*2978T>C
ENST00000512095.5:n.2395T>C
NM_025132.3:c.3397T>C	NP_079408.3:p.Tyr1133His
XM_011513724.1:c.3409T>C	XP_011512026.1:p.Tyr1137His
XM_011513725.1:c.3343T>C	XP_011512027.1:p.Tyr1115His
XM_011513726.1:c.2929T>C	XP_011512028.1:p.Tyr977His
XM_011513727.1:c.2929T>C	XP_011512029.1:p.Tyr977His
XM_011513728.1:c.2917T>C	XP_011512030.1:p.Tyr973His
XR_925155.1:n.3473T>C
NM_001317924.1:c.2917T>C	NP_001304853.1:p.Tyr973His
XM_011513725.2:c.3343T>C	XP_011512027.1:p.Tyr1115His
XM_011513726.3:c.2929T>C	XP_011512028.1:p.Tyr977His
XM_017008501.1:c.2917T>C	XP_016863990.1:p.Tyr973His
XR_001741306.1:n.3473T>C
XR_001741307.1:n.3461T>C
XR_001741308.1:n.3473T>C
XR_001741309.1:n.3461T>C
XR_001741310.1:n.3461T>C
XR_001741311.2:n.3310T>C
NM_025132.4:c.3397T>C MANE Select	NP_079408.3:p.Tyr1133His
NM_001317924.2:c.2917T>C	NP_001304853.1:p.Tyr973His