Canonical Allele Identifier: CA356637470

Gene: WDR19

Linked Data

• MyVariant Identifiers: chr4:g.39245976A>T (hg19) ; chr4:g.39244356A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244356A>T , CM000666.2:g.39244356A>T	GRCh38
NC_000004.11:g.39245976A>T , CM000666.1:g.39245976A>T	GRCh37
NC_000004.10:g.38922371A>T	NCBI36
NG_031813.1:g.66953A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2530A>T MANE Select	ENSP00000382717.3:p.Arg844Ter
ENST00000399820.7:c.2530A>T	ENSP00000382717.3:p.Arg844Ter
ENST00000506869.5:c.*2111A>T	ENSP00000424319.1:n.*2111A>T
ENST00000512095.5:n.1528A>T
NM_025132.3:c.2530A>T	NP_079408.3:p.Arg844Ter
XM_011513724.1:c.2542A>T	XP_011512026.1:p.Arg848Ter
XM_011513725.1:c.2476A>T	XP_011512027.1:p.Arg826Ter
XM_011513726.1:c.2062A>T	XP_011512028.1:p.Arg688Ter
XM_011513727.1:c.2062A>T	XP_011512029.1:p.Arg688Ter
XM_011513728.1:c.2050A>T	XP_011512030.1:p.Arg684Ter
XM_011513729.1:c.2542A>T	XP_011512031.1:p.Arg848Ter
XR_925155.1:n.2606A>T
NM_001317924.1:c.2050A>T	NP_001304853.1:p.Arg684Ter
XM_011513725.2:c.2476A>T	XP_011512027.1:p.Arg826Ter
XM_011513726.3:c.2062A>T	XP_011512028.1:p.Arg688Ter
XM_017008501.1:c.2050A>T	XP_016863990.1:p.Arg684Ter
XR_001741306.1:n.2606A>T
XR_001741307.1:n.2594A>T
XR_001741308.1:n.2606A>T
XR_001741309.1:n.2594A>T
XR_001741310.1:n.2594A>T
XR_001741311.2:n.2443A>T
NM_025132.4:c.2530A>T MANE Select	NP_079408.3:p.Arg844Ter
NM_001317924.2:c.2050A>T	NP_001304853.1:p.Arg684Ter