Canonical Allele Identifier: CA356634464

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207296A>T (hg19) ; chr4:g.39205676A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205676A>T , CM000666.2:g.39205676A>T	GRCh38
NC_000004.11:g.39207296A>T , CM000666.1:g.39207296A>T	GRCh37
NC_000004.10:g.38883691A>T	NCBI36
NG_031813.1:g.28273A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.830A>T MANE Select	ENSP00000382717.3:p.Asn277Ile
ENST00000399820.7:c.830A>T	ENSP00000382717.3:p.Asn277Ile
ENST00000503697.5:c.*298A>T	ENSP00000423706.1:n.*298A>T
ENST00000506503.1:c.830A>T	ENSP00000423491.1:p.Asn277Ile
ENST00000506869.5:c.*411A>T	ENSP00000424319.1:n.*411A>T
ENST00000511729.5:n.41-22882A>T
ENST00000512448.1:n.424A>T
NM_025132.3:c.830A>T	NP_079408.3:p.Asn277Ile
XM_011513724.1:c.830A>T	XP_011512026.1:p.Asn277Ile
XM_011513725.1:c.764A>T	XP_011512027.1:p.Asn255Ile
XM_011513726.1:c.350A>T	XP_011512028.1:p.Asn117Ile
XM_011513727.1:c.350A>T	XP_011512029.1:p.Asn117Ile
XM_011513728.1:c.350A>T	XP_011512030.1:p.Asn117Ile
XM_011513729.1:c.830A>T	XP_011512031.1:p.Asn277Ile
XR_925155.1:n.894A>T
NM_001317924.1:c.350A>T	NP_001304853.1:p.Asn117Ile
XM_011513725.2:c.764A>T	XP_011512027.1:p.Asn255Ile
XM_011513726.3:c.350A>T	XP_011512028.1:p.Asn117Ile
XM_017008501.1:c.350A>T	XP_016863990.1:p.Asn117Ile
XR_001741306.1:n.894A>T
XR_001741307.1:n.894A>T
XR_001741308.1:n.894A>T
XR_001741309.1:n.894A>T
XR_001741310.1:n.894A>T
XR_001741311.2:n.743A>T
XR_001741312.1:n.894A>T
NM_025132.4:c.830A>T MANE Select	NP_079408.3:p.Asn277Ile
NM_001317924.2:c.350A>T	NP_001304853.1:p.Asn117Ile