Canonical Allele Identifier: CA356652273

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278725C>G (hg19) ; chr4:g.39277105C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277105C>G , CM000666.2:g.39277105C>G	GRCh38
NC_000004.11:g.39278725C>G , CM000666.1:g.39278725C>G	GRCh37
NC_000004.10:g.38955120C>G	NCBI36
NG_031813.1:g.99702C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3802C>G MANE Select	ENSP00000382717.3:p.Pro1268Ala
ENST00000399820.7:c.3802C>G	ENSP00000382717.3:p.Pro1268Ala
ENST00000503733.1:n.142C>G
ENST00000506869.5:c.*3383C>G	ENSP00000424319.1:n.*3383C>G
ENST00000512534.5:n.2113C>G
ENST00000512588.5:n.144C>G
NM_025132.3:c.3802C>G	NP_079408.3:p.Pro1268Ala
XM_011513724.1:c.3814C>G	XP_011512026.1:p.Pro1272Ala
XM_011513725.1:c.3748C>G	XP_011512027.1:p.Pro1250Ala
XM_011513726.1:c.3334C>G	XP_011512028.1:p.Pro1112Ala
XM_011513727.1:c.3334C>G	XP_011512029.1:p.Pro1112Ala
XM_011513728.1:c.3322C>G	XP_011512030.1:p.Pro1108Ala
XR_925155.1:n.5512C>G
NM_001317924.1:c.3322C>G	NP_001304853.1:p.Pro1108Ala
XM_011513725.2:c.3748C>G	XP_011512027.1:p.Pro1250Ala
XM_011513726.3:c.3334C>G	XP_011512028.1:p.Pro1112Ala
XM_017008501.1:c.3322C>G	XP_016863990.1:p.Pro1108Ala
XR_001741306.1:n.4079C>G
XR_001741307.1:n.4067C>G
XR_001741308.1:n.5713C>G
XR_001741309.1:n.5500C>G
XR_001741310.1:n.5701C>G
XR_001741311.2:n.5349C>G
NM_025132.4:c.3802C>G MANE Select	NP_079408.3:p.Pro1268Ala
NM_001317924.2:c.3322C>G	NP_001304853.1:p.Pro1108Ala