Canonical Allele Identifier: CA356637435

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245961A>G (hg19) ; chr4:g.39244341A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244341A>G , CM000666.2:g.39244341A>G	GRCh38
NC_000004.11:g.39245961A>G , CM000666.1:g.39245961A>G	GRCh37
NC_000004.10:g.38922356A>G	NCBI36
NG_031813.1:g.66938A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2515A>G MANE Select	ENSP00000382717.3:p.Ser839Gly
ENST00000399820.7:c.2515A>G	ENSP00000382717.3:p.Ser839Gly
ENST00000506869.5:c.*2096A>G	ENSP00000424319.1:n.*2096A>G
ENST00000512095.5:n.1513A>G
NM_025132.3:c.2515A>G	NP_079408.3:p.Ser839Gly
XM_011513724.1:c.2527A>G	XP_011512026.1:p.Ser843Gly
XM_011513725.1:c.2461A>G	XP_011512027.1:p.Ser821Gly
XM_011513726.1:c.2047A>G	XP_011512028.1:p.Ser683Gly
XM_011513727.1:c.2047A>G	XP_011512029.1:p.Ser683Gly
XM_011513728.1:c.2035A>G	XP_011512030.1:p.Ser679Gly
XM_011513729.1:c.2527A>G	XP_011512031.1:p.Ser843Gly
XR_925155.1:n.2591A>G
NM_001317924.1:c.2035A>G	NP_001304853.1:p.Ser679Gly
XM_011513725.2:c.2461A>G	XP_011512027.1:p.Ser821Gly
XM_011513726.3:c.2047A>G	XP_011512028.1:p.Ser683Gly
XM_017008501.1:c.2035A>G	XP_016863990.1:p.Ser679Gly
XR_001741306.1:n.2591A>G
XR_001741307.1:n.2579A>G
XR_001741308.1:n.2591A>G
XR_001741309.1:n.2579A>G
XR_001741310.1:n.2579A>G
XR_001741311.2:n.2428A>G
NM_025132.4:c.2515A>G MANE Select	NP_079408.3:p.Ser839Gly
NM_001317924.2:c.2035A>G	NP_001304853.1:p.Ser679Gly