Canonical Allele Identifier: CA2761116312

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274976T>C , CM000666.2:g.39274976T>C	GRCh38
NC_000004.11:g.39276596T>C , CM000666.1:g.39276596T>C	GRCh37
NC_000004.10:g.38952991T>C	NCBI36
NG_031813.1:g.97573T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+18T>C MANE Select	ENSP00000382717.3:n.3716+18T>C
ENST00000399820.7:c.3716+18T>C	ENSP00000382717.3:n.3716+18T>C
ENST00000506869.5:c.*3297+18T>C	ENSP00000424319.1:n.*3297+18T>C
ENST00000512095.5:n.2732T>C
ENST00000512534.5:n.2027+18T>C
NM_025132.3:c.3716+18T>C	NP_079408.3:n.3716+18T>C
XM_011513724.1:c.3728+18T>C	XP_011512026.1:n.3728+18T>C
XM_011513725.1:c.3662+18T>C	XP_011512027.1:n.3662+18T>C
XM_011513726.1:c.3248+18T>C	XP_011512028.1:n.3248+18T>C
XM_011513727.1:c.3248+18T>C	XP_011512029.1:n.3248+18T>C
XM_011513728.1:c.3236+18T>C	XP_011512030.1:n.3236+18T>C
XR_925155.1:n.5426+18T>C
NM_001317924.1:c.3236+18T>C	NP_001304853.1:n.3236+18T>C
XM_011513725.2:c.3662+18T>C	XP_011512027.1:n.3662+18T>C
XM_011513726.3:c.3248+18T>C	XP_011512028.1:n.3248+18T>C
XM_017008501.1:c.3236+18T>C	XP_016863990.1:n.3236+18T>C
XR_001741306.1:n.3792+18T>C
XR_001741307.1:n.3780+18T>C
XR_001741308.1:n.5426+18T>C
XR_001741309.1:n.5414+18T>C
XR_001741310.1:n.5414+18T>C
XR_001741311.2:n.5263+18T>C
NM_025132.4:c.3716+18T>C MANE Select	NP_079408.3:n.3716+18T>C
NM_001317924.2:c.3236+18T>C	NP_001304853.1:n.3236+18T>C