Canonical Allele Identifier: CA356634489

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39207308T>A (hg19) ; chr4:g.39205688T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205688T>A , CM000666.2:g.39205688T>A	GRCh38
NC_000004.11:g.39207308T>A , CM000666.1:g.39207308T>A	GRCh37
NC_000004.10:g.38883703T>A	NCBI36
NG_031813.1:g.28285T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.842T>A MANE Select	ENSP00000382717.3:p.Ile281Asn
ENST00000399820.7:c.842T>A	ENSP00000382717.3:p.Ile281Asn
ENST00000503697.5:c.*310T>A	ENSP00000423706.1:n.*310T>A
ENST00000506503.1:c.842T>A	ENSP00000423491.1:p.Ile281Asn
ENST00000506869.5:c.*423T>A	ENSP00000424319.1:n.*423T>A
ENST00000511729.5:n.41-22870T>A
ENST00000512448.1:n.436T>A
NM_025132.3:c.842T>A	NP_079408.3:p.Ile281Asn
XM_011513724.1:c.842T>A	XP_011512026.1:p.Ile281Asn
XM_011513725.1:c.776T>A	XP_011512027.1:p.Ile259Asn
XM_011513726.1:c.362T>A	XP_011512028.1:p.Ile121Asn
XM_011513727.1:c.362T>A	XP_011512029.1:p.Ile121Asn
XM_011513728.1:c.362T>A	XP_011512030.1:p.Ile121Asn
XM_011513729.1:c.842T>A	XP_011512031.1:p.Ile281Asn
XR_925155.1:n.906T>A
NM_001317924.1:c.362T>A	NP_001304853.1:p.Ile121Asn
XM_011513725.2:c.776T>A	XP_011512027.1:p.Ile259Asn
XM_011513726.3:c.362T>A	XP_011512028.1:p.Ile121Asn
XM_017008501.1:c.362T>A	XP_016863990.1:p.Ile121Asn
XR_001741306.1:n.906T>A
XR_001741307.1:n.906T>A
XR_001741308.1:n.906T>A
XR_001741309.1:n.906T>A
XR_001741310.1:n.906T>A
XR_001741311.2:n.755T>A
XR_001741312.1:n.906T>A
NM_025132.4:c.842T>A MANE Select	NP_079408.3:p.Ile281Asn
NM_001317924.2:c.362T>A	NP_001304853.1:p.Ile121Asn