Canonical Allele Identifier: CA356638721

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39246158C>G (hg19) ; chr4:g.39244538C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244538C>G , CM000666.2:g.39244538C>G	GRCh38
NC_000004.11:g.39246158C>G , CM000666.1:g.39246158C>G	GRCh37
NC_000004.10:g.38922553C>G	NCBI36
NG_031813.1:g.67135C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2631C>G MANE Select	ENSP00000382717.3:p.Ile877Met
ENST00000399820.7:c.2631C>G	ENSP00000382717.3:p.Ile877Met
ENST00000506869.5:c.*2212C>G	ENSP00000424319.1:n.*2212C>G
ENST00000512095.5:n.1629C>G
NM_025132.3:c.2631C>G	NP_079408.3:p.Ile877Met
XM_011513724.1:c.2643C>G	XP_011512026.1:p.Ile881Met
XM_011513725.1:c.2577C>G	XP_011512027.1:p.Ile859Met
XM_011513726.1:c.2163C>G	XP_011512028.1:p.Ile721Met
XM_011513727.1:c.2163C>G	XP_011512029.1:p.Ile721Met
XM_011513728.1:c.2151C>G	XP_011512030.1:p.Ile717Met
XM_011513729.1:c.2643C>G	XP_011512031.1:p.Ile881Met
XR_925155.1:n.2707C>G
NM_001317924.1:c.2151C>G	NP_001304853.1:p.Ile717Met
XM_011513725.2:c.2577C>G	XP_011512027.1:p.Ile859Met
XM_011513726.3:c.2163C>G	XP_011512028.1:p.Ile721Met
XM_017008501.1:c.2151C>G	XP_016863990.1:p.Ile717Met
XR_001741306.1:n.2707C>G
XR_001741307.1:n.2695C>G
XR_001741308.1:n.2707C>G
XR_001741309.1:n.2695C>G
XR_001741310.1:n.2695C>G
XR_001741311.2:n.2544C>G
NM_025132.4:c.2631C>G MANE Select	NP_079408.3:p.Ile877Met
NM_001317924.2:c.2151C>G	NP_001304853.1:p.Ile717Met