Canonical Allele Identifier: CA2892191

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39253198A>T , CM000666.2:g.39253198A>T	GRCh38
NC_000004.11:g.39254818A>T , CM000666.1:g.39254818A>T	GRCh37
NC_000004.10:g.38931213A>T	NCBI36
NG_031813.1:g.75795A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025132.4:c.2782A>T MANE Select	NP_079408.3:p.Ile928Phe
ENST00000399820.8:c.2782A>T MANE Select	ENSP00000382717.3:p.Ile928Phe
NM_001317924.1:c.2302A>T	NP_001304853.1:p.Ile768Phe
NM_001317924.2:c.2302A>T	NP_001304853.1:p.Ile768Phe
NM_025132.3:c.2782A>T	NP_079408.3:p.Ile928Phe
ENST00000399820.7:c.2782A>T	ENSP00000382717.3:p.Ile928Phe
ENST00000506869.5:c.*2363A>T	ENSP00000424319.1:n.*2363A>T
ENST00000512095.5:n.1780A>T
XM_011513724.1:c.2794A>T	XP_011512026.1:p.Ile932Phe
XM_011513725.1:c.2728A>T	XP_011512027.1:p.Ile910Phe
XM_011513725.2:c.2728A>T	XP_011512027.1:p.Ile910Phe
XM_011513726.1:c.2314A>T	XP_011512028.1:p.Ile772Phe
XM_011513726.3:c.2314A>T	XP_011512028.1:p.Ile772Phe
XM_011513727.1:c.2314A>T	XP_011512029.1:p.Ile772Phe
XM_011513728.1:c.2302A>T	XP_011512030.1:p.Ile768Phe
XM_011513729.1:c.2794A>T	XP_011512031.1:p.Ile932Phe
XM_017008501.1:c.2302A>T	XP_016863990.1:p.Ile768Phe
XR_001741306.1:n.2858A>T
XR_001741307.1:n.2846A>T
XR_001741308.1:n.2858A>T
XR_001741309.1:n.2846A>T
XR_001741310.1:n.2846A>T
XR_001741311.2:n.2695A>T
XR_925155.1:n.2858A>T