Canonical Allele Identifier: CA356652359

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39278737A>G (hg19) ; chr4:g.39277117A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277117A>G , CM000666.2:g.39277117A>G	GRCh38
NC_000004.11:g.39278737A>G , CM000666.1:g.39278737A>G	GRCh37
NC_000004.10:g.38955132A>G	NCBI36
NG_031813.1:g.99714A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3814A>G MANE Select	ENSP00000382717.3:p.Asn1272Asp
ENST00000399820.7:c.3814A>G	ENSP00000382717.3:p.Asn1272Asp
ENST00000503733.1:n.154A>G
ENST00000506869.5:c.*3395A>G	ENSP00000424319.1:n.*3395A>G
ENST00000512534.5:n.2125A>G
ENST00000512588.5:n.156A>G
NM_025132.3:c.3814A>G	NP_079408.3:p.Asn1272Asp
XM_011513724.1:c.3826A>G	XP_011512026.1:p.Asn1276Asp
XM_011513725.1:c.3760A>G	XP_011512027.1:p.Asn1254Asp
XM_011513726.1:c.3346A>G	XP_011512028.1:p.Asn1116Asp
XM_011513727.1:c.3346A>G	XP_011512029.1:p.Asn1116Asp
XM_011513728.1:c.3334A>G	XP_011512030.1:p.Asn1112Asp
XR_925155.1:n.5524A>G
NM_001317924.1:c.3334A>G	NP_001304853.1:p.Asn1112Asp
XM_011513725.2:c.3760A>G	XP_011512027.1:p.Asn1254Asp
XM_011513726.3:c.3346A>G	XP_011512028.1:p.Asn1116Asp
XM_017008501.1:c.3334A>G	XP_016863990.1:p.Asn1112Asp
XR_001741306.1:n.4091A>G
XR_001741307.1:n.4079A>G
XR_001741308.1:n.5725A>G
XR_001741309.1:n.5512A>G
XR_001741310.1:n.5713A>G
XR_001741311.2:n.5361A>G
NM_025132.4:c.3814A>G MANE Select	NP_079408.3:p.Asn1272Asp
NM_001317924.2:c.3334A>G	NP_001304853.1:p.Asn1112Asp