Canonical Allele Identifier: CA356638212

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246091A>T (hg19) ; chr4:g.39244471A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244471A>T , CM000666.2:g.39244471A>T	GRCh38
NC_000004.11:g.39246091A>T , CM000666.1:g.39246091A>T	GRCh37
NC_000004.10:g.38922486A>T	NCBI36
NG_031813.1:g.67068A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2564A>T MANE Select	ENSP00000382717.3:p.Gln855Leu
ENST00000399820.7:c.2564A>T	ENSP00000382717.3:p.Gln855Leu
ENST00000506869.5:c.*2145A>T	ENSP00000424319.1:n.*2145A>T
ENST00000512095.5:n.1562A>T
NM_025132.3:c.2564A>T	NP_079408.3:p.Gln855Leu
XM_011513724.1:c.2576A>T	XP_011512026.1:p.Gln859Leu
XM_011513725.1:c.2510A>T	XP_011512027.1:p.Gln837Leu
XM_011513726.1:c.2096A>T	XP_011512028.1:p.Gln699Leu
XM_011513727.1:c.2096A>T	XP_011512029.1:p.Gln699Leu
XM_011513728.1:c.2084A>T	XP_011512030.1:p.Gln695Leu
XM_011513729.1:c.2576A>T	XP_011512031.1:p.Gln859Leu
XR_925155.1:n.2640A>T
NM_001317924.1:c.2084A>T	NP_001304853.1:p.Gln695Leu
XM_011513725.2:c.2510A>T	XP_011512027.1:p.Gln837Leu
XM_011513726.3:c.2096A>T	XP_011512028.1:p.Gln699Leu
XM_017008501.1:c.2084A>T	XP_016863990.1:p.Gln695Leu
XR_001741306.1:n.2640A>T
XR_001741307.1:n.2628A>T
XR_001741308.1:n.2640A>T
XR_001741309.1:n.2628A>T
XR_001741310.1:n.2628A>T
XR_001741311.2:n.2477A>T
NM_025132.4:c.2564A>T MANE Select	NP_079408.3:p.Gln855Leu
NM_001317924.2:c.2084A>T	NP_001304853.1:p.Gln695Leu