Canonical Allele Identifier: CA438942092

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246143A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244523A>C , CM000666.2:g.39244523A>C	GRCh38
NC_000004.11:g.39246143A>C , CM000666.1:g.39246143A>C	GRCh37
NC_000004.10:g.38922538A>C	NCBI36
NG_031813.1:g.67120A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2616A>C MANE Select	ENSP00000382717.3:p.Ala872=
ENST00000399820.7:c.2616A>C	ENSP00000382717.3:p.Ala872=
ENST00000506869.5:c.*2197A>C	ENSP00000424319.1:n.*2197A>C
ENST00000512095.5:n.1614A>C
NM_025132.3:c.2616A>C	NP_079408.3:p.Ala872=
XM_011513724.1:c.2628A>C	XP_011512026.1:p.Ala876=
XM_011513725.1:c.2562A>C	XP_011512027.1:p.Ala854=
XM_011513726.1:c.2148A>C	XP_011512028.1:p.Ala716=
XM_011513727.1:c.2148A>C	XP_011512029.1:p.Ala716=
XM_011513728.1:c.2136A>C	XP_011512030.1:p.Ala712=
XM_011513729.1:c.2628A>C	XP_011512031.1:p.Ala876=
XR_925155.1:n.2692A>C
NM_001317924.1:c.2136A>C	NP_001304853.1:p.Ala712=
XM_011513725.2:c.2562A>C	XP_011512027.1:p.Ala854=
XM_011513726.3:c.2148A>C	XP_011512028.1:p.Ala716=
XM_017008501.1:c.2136A>C	XP_016863990.1:p.Ala712=
XR_001741306.1:n.2692A>C
XR_001741307.1:n.2680A>C
XR_001741308.1:n.2692A>C
XR_001741309.1:n.2680A>C
XR_001741310.1:n.2680A>C
XR_001741311.2:n.2529A>C
NM_025132.4:c.2616A>C MANE Select	NP_079408.3:p.Ala872=
NM_001317924.2:c.2136A>C	NP_001304853.1:p.Ala712=