Canonical Allele Identifier: CA356636295

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39214673T>C , CM000666.2:g.39214673T>C	GRCh38
NC_000004.11:g.39216293T>C , CM000666.1:g.39216293T>C	GRCh37
NC_000004.10:g.38892688T>C	NCBI36
NG_031813.1:g.37270T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.961+2T>C MANE Select	NP_079408.3:n.961+2T>C
ENST00000399820.8:c.961+2T>C MANE Select	ENSP00000382717.3:n.961+2T>C
NM_001317924.1:c.481+2T>C	NP_001304853.1:n.481+2T>C
NM_001317924.2:c.481+2T>C	NP_001304853.1:n.481+2T>C
NM_025132.3:c.961+2T>C	NP_079408.3:n.961+2T>C
ENST00000399820.7:c.961+2T>C	ENSP00000382717.3:n.961+2T>C
ENST00000503697.5:c.*429+2T>C	ENSP00000423706.1:n.*429+2T>C
ENST00000506503.1:c.961+2T>C	ENSP00000423491.1:n.961+2T>C
ENST00000506869.5:c.*542+2T>C	ENSP00000424319.1:n.*542+2T>C
ENST00000511729.5:n.41-13885T>C
XM_011513724.1:c.961+2T>C	XP_011512026.1:n.961+2T>C
XM_011513725.1:c.895+2T>C	XP_011512027.1:n.895+2T>C
XM_011513725.2:c.895+2T>C	XP_011512027.1:n.895+2T>C
XM_011513726.1:c.481+2T>C	XP_011512028.1:n.481+2T>C
XM_011513726.3:c.481+2T>C	XP_011512028.1:n.481+2T>C
XM_011513727.1:c.481+2T>C	XP_011512029.1:n.481+2T>C
XM_011513728.1:c.481+2T>C	XP_011512030.1:n.481+2T>C
XM_011513729.1:c.961+2T>C	XP_011512031.1:n.961+2T>C
XM_017008501.1:c.481+2T>C	XP_016863990.1:n.481+2T>C
XR_001741306.1:n.1025+2T>C
XR_001741307.1:n.1025+2T>C
XR_001741308.1:n.1025+2T>C
XR_001741309.1:n.1025+2T>C
XR_001741310.1:n.1025+2T>C
XR_001741311.2:n.874+2T>C
XR_001741312.1:n.1025+2T>C
XR_925155.1:n.1025+2T>C