Canonical Allele Identifier: CA2670361375

Gene: WDR19

Linked Data

• gnomAD v4: 4-39272954-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39272954A>C , CM000666.2:g.39272954A>C	GRCh38
NC_000004.11:g.39274574A>C , CM000666.1:g.39274574A>C	GRCh37
NC_000004.10:g.38950969A>C	NCBI36
NG_031813.1:g.95551A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3484-26A>C MANE Select	ENSP00000382717.3:n.3484-26A>C
ENST00000399820.7:c.3484-26A>C	ENSP00000382717.3:n.3484-26A>C
ENST00000506869.5:c.*3065-26A>C	ENSP00000424319.1:n.*3065-26A>C
ENST00000512095.5:n.2482-26A>C
ENST00000512534.5:n.49-26A>C
NM_025132.3:c.3484-26A>C	NP_079408.3:n.3484-26A>C
XM_011513724.1:c.3496-26A>C	XP_011512026.1:n.3496-26A>C
XM_011513725.1:c.3430-26A>C	XP_011512027.1:n.3430-26A>C
XM_011513726.1:c.3016-26A>C	XP_011512028.1:n.3016-26A>C
XM_011513727.1:c.3016-26A>C	XP_011512029.1:n.3016-26A>C
XM_011513728.1:c.3004-26A>C	XP_011512030.1:n.3004-26A>C
XR_925155.1:n.3560-26A>C
NM_001317924.1:c.3004-26A>C	NP_001304853.1:n.3004-26A>C
XM_011513725.2:c.3430-26A>C	XP_011512027.1:n.3430-26A>C
XM_011513726.3:c.3016-26A>C	XP_011512028.1:n.3016-26A>C
XM_017008501.1:c.3004-26A>C	XP_016863990.1:n.3004-26A>C
XR_001741306.1:n.3560-26A>C
XR_001741307.1:n.3548-26A>C
XR_001741308.1:n.3560-26A>C
XR_001741309.1:n.3548-26A>C
XR_001741310.1:n.3548-26A>C
XR_001741311.2:n.3397-26A>C
NM_025132.4:c.3484-26A>C MANE Select	NP_079408.3:n.3484-26A>C
NM_001317924.2:c.3004-26A>C	NP_001304853.1:n.3004-26A>C