Canonical Allele Identifier: CA2761116397

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275022_39275023insAC , CM000666.2:g.39275022_39275023insAC	GRCh38
NC_000004.11:g.39276642_39276643insAC , CM000666.1:g.39276642_39276643insAC	GRCh37
NC_000004.10:g.38953037_38953038insAC	NCBI36
NG_031813.1:g.97619_97620insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+64_3716+65insAC MANE Select	ENSP00000382717.3:n.3716+64_3716+65insAC
ENST00000399820.7:c.3716+64_3716+65insAC	ENSP00000382717.3:n.3716+64_3716+65insAC
ENST00000506869.5:c.*3297+64_*3297+65insAC	ENSP00000424319.1:n.*3297+64_*3297+65insAC
ENST00000512095.5:n.2778_2779insAC
ENST00000512534.5:n.2027+64_2027+65insAC
NM_025132.3:c.3716+64_3716+65insAC	NP_079408.3:n.3716+64_3716+65insAC
XM_011513724.1:c.3728+64_3728+65insAC	XP_011512026.1:n.3728+64_3728+65insAC
XM_011513725.1:c.3662+64_3662+65insAC	XP_011512027.1:n.3662+64_3662+65insAC
XM_011513726.1:c.3248+64_3248+65insAC	XP_011512028.1:n.3248+64_3248+65insAC
XM_011513727.1:c.3248+64_3248+65insAC	XP_011512029.1:n.3248+64_3248+65insAC
XM_011513728.1:c.3236+64_3236+65insAC	XP_011512030.1:n.3236+64_3236+65insAC
XR_925155.1:n.5426+64_5426+65insAC
NM_001317924.1:c.3236+64_3236+65insAC	NP_001304853.1:n.3236+64_3236+65insAC
XM_011513725.2:c.3662+64_3662+65insAC	XP_011512027.1:n.3662+64_3662+65insAC
XM_011513726.3:c.3248+64_3248+65insAC	XP_011512028.1:n.3248+64_3248+65insAC
XM_017008501.1:c.3236+64_3236+65insAC	XP_016863990.1:n.3236+64_3236+65insAC
XR_001741306.1:n.3792+64_3792+65insAC
XR_001741307.1:n.3780+64_3780+65insAC
XR_001741308.1:n.5426+64_5426+65insAC
XR_001741309.1:n.5414+64_5414+65insAC
XR_001741310.1:n.5414+64_5414+65insAC
XR_001741311.2:n.5263+64_5263+65insAC
NM_025132.4:c.3716+64_3716+65insAC MANE Select	NP_079408.3:n.3716+64_3716+65insAC
NM_001317924.2:c.3236+64_3236+65insAC	NP_001304853.1:n.3236+64_3236+65insAC