Canonical Allele Identifier: CA438939418
Gene: WDR19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.39207291A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205671A>G , CM000666.2:g.39205671A>G GRCh38
NC_000004.11:g.39207291A>G , CM000666.1:g.39207291A>G GRCh37
NC_000004.10:g.38883686A>G NCBI36
NG_031813.1:g.28268A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.825A>G MANE Select ENSP00000382717.3:p.Lys275=
ENST00000399820.7:c.825A>G ENSP00000382717.3:p.Lys275=
ENST00000503697.5:c.*293A>G ENSP00000423706.1:n.*293A>G
ENST00000506503.1:c.825A>G ENSP00000423491.1:p.Lys275=
ENST00000506869.5:c.*406A>G ENSP00000424319.1:n.*406A>G
ENST00000511729.5:n.41-22887A>G
ENST00000512448.1:n.419A>G
NM_025132.3:c.825A>G NP_079408.3:p.Lys275=
XM_011513724.1:c.825A>G XP_011512026.1:p.Lys275=
XM_011513725.1:c.759A>G XP_011512027.1:p.Lys253=
XM_011513726.1:c.345A>G XP_011512028.1:p.Lys115=
XM_011513727.1:c.345A>G XP_011512029.1:p.Lys115=
XM_011513728.1:c.345A>G XP_011512030.1:p.Lys115=
XM_011513729.1:c.825A>G XP_011512031.1:p.Lys275=
XR_925155.1:n.889A>G
NM_001317924.1:c.345A>G NP_001304853.1:p.Lys115=
XM_011513725.2:c.759A>G XP_011512027.1:p.Lys253=
XM_011513726.3:c.345A>G XP_011512028.1:p.Lys115=
XM_017008501.1:c.345A>G XP_016863990.1:p.Lys115=
XR_001741306.1:n.889A>G
XR_001741307.1:n.889A>G
XR_001741308.1:n.889A>G
XR_001741309.1:n.889A>G
XR_001741310.1:n.889A>G
XR_001741311.2:n.738A>G
XR_001741312.1:n.889A>G
NM_025132.4:c.825A>G MANE Select NP_079408.3:p.Lys275=
NM_001317924.2:c.345A>G NP_001304853.1:p.Lys115=