Canonical Allele Identifier: CA2891890

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39225011G>C , CM000666.2:g.39225011G>C	GRCh38
NC_000004.11:g.39226631G>C , CM000666.1:g.39226631G>C	GRCh37
NC_000004.10:g.38903026G>C	NCBI36
NG_031813.1:g.47608G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.1607G>C MANE Select	ENSP00000382717.3:p.Ser536Thr
ENST00000399820.7:c.1607G>C	ENSP00000382717.3:p.Ser536Thr
ENST00000506869.5:c.*1188G>C	ENSP00000424319.1:n.*1188G>C
ENST00000511729.5:n.41-3547G>C
ENST00000512095.5:n.605G>C
NM_025132.3:c.1607G>C	NP_079408.3:p.Ser536Thr
XM_011513724.1:c.1607G>C	XP_011512026.1:p.Ser536Thr
XM_011513725.1:c.1541G>C	XP_011512027.1:p.Ser514Thr
XM_011513726.1:c.1127G>C	XP_011512028.1:p.Ser376Thr
XM_011513727.1:c.1127G>C	XP_011512029.1:p.Ser376Thr
XM_011513728.1:c.1127G>C	XP_011512030.1:p.Ser376Thr
XM_011513729.1:c.1607G>C	XP_011512031.1:p.Ser536Thr
XR_925155.1:n.1671G>C
NM_001317924.1:c.1127G>C	NP_001304853.1:p.Ser376Thr
XM_011513725.2:c.1541G>C	XP_011512027.1:p.Ser514Thr
XM_011513726.3:c.1127G>C	XP_011512028.1:p.Ser376Thr
XM_017008501.1:c.1127G>C	XP_016863990.1:p.Ser376Thr
XR_001741306.1:n.1671G>C
XR_001741307.1:n.1671G>C
XR_001741308.1:n.1671G>C
XR_001741309.1:n.1671G>C
XR_001741310.1:n.1671G>C
XR_001741311.2:n.1520G>C
XR_001741312.1:n.1671G>C
NM_025132.4:c.1607G>C MANE Select	NP_079408.3:p.Ser536Thr
NM_001317924.2:c.1127G>C	NP_001304853.1:p.Ser376Thr