Canonical Allele Identifier: CA2670359618

Gene: WDR19

Linked Data

• gnomAD v4: 4-39244611-TCTCCCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244614_39244620del , CM000666.2:g.39244614_39244620del	GRCh38
NC_000004.11:g.39246234_39246240del , CM000666.1:g.39246234_39246240del	GRCh37
NC_000004.10:g.38922629_38922635del	NCBI36
NG_031813.1:g.67211_67217del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2645+62_2645+68del MANE Select	ENSP00000382717.3:n.2645+62_2645+68del
ENST00000399820.7:c.2645+62_2645+68del	ENSP00000382717.3:n.2645+62_2645+68del
ENST00000506869.5:c.*2226+62_*2226+68del	ENSP00000424319.1:n.*2226+62_*2226+68del
ENST00000512095.5:n.1643+62_1643+68del
NM_025132.3:c.2645+62_2645+68del	NP_079408.3:n.2645+62_2645+68del
XM_011513724.1:c.2657+62_2657+68del	XP_011512026.1:n.2657+62_2657+68del
XM_011513725.1:c.2591+62_2591+68del	XP_011512027.1:n.2591+62_2591+68del
XM_011513726.1:c.2177+62_2177+68del	XP_011512028.1:n.2177+62_2177+68del
XM_011513727.1:c.2177+62_2177+68del	XP_011512029.1:n.2177+62_2177+68del
XM_011513728.1:c.2165+62_2165+68del	XP_011512030.1:n.2165+62_2165+68del
XM_011513729.1:c.2657+62_2657+68del	XP_011512031.1:n.2657+62_2657+68del
XR_925155.1:n.2721+62_2721+68del
NM_001317924.1:c.2165+62_2165+68del	NP_001304853.1:n.2165+62_2165+68del
XM_011513725.2:c.2591+62_2591+68del	XP_011512027.1:n.2591+62_2591+68del
XM_011513726.3:c.2177+62_2177+68del	XP_011512028.1:n.2177+62_2177+68del
XM_017008501.1:c.2165+62_2165+68del	XP_016863990.1:n.2165+62_2165+68del
XR_001741306.1:n.2721+62_2721+68del
XR_001741307.1:n.2709+62_2709+68del
XR_001741308.1:n.2721+62_2721+68del
XR_001741309.1:n.2709+62_2709+68del
XR_001741310.1:n.2709+62_2709+68del
XR_001741311.2:n.2558+62_2558+68del
NM_025132.4:c.2645+62_2645+68del MANE Select	NP_079408.3:n.2645+62_2645+68del
NM_001317924.2:c.2165+62_2165+68del	NP_001304853.1:n.2165+62_2165+68del