Canonical Allele Identifier: CA794675110

Gene: WDR19

Linked Data

• dbSNP Id: rs1197070628
• MyVariant Identifiers: chr4:g.39276726_39276728del (hg19) ; chr4:g.39275106_39275108del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275107_39275109del , CM000666.2:g.39275107_39275109del	GRCh38
NC_000004.11:g.39276727_39276729del , CM000666.1:g.39276727_39276729del	GRCh37
NC_000004.10:g.38953122_38953124del	NCBI36
NG_031813.1:g.97704_97706del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+149_3716+151del MANE Select	ENSP00000382717.3:n.3716+149_3716+151del
ENST00000399820.7:c.3716+149_3716+151del	ENSP00000382717.3:n.3716+149_3716+151del
ENST00000506869.5:c.*3297+149_*3297+151del	ENSP00000424319.1:n.*3297+149_*3297+151del
ENST00000512095.5:n.2863_2865del
ENST00000512534.5:n.2027+149_2027+151del
NM_025132.3:c.3716+149_3716+151del	NP_079408.3:n.3716+149_3716+151del
XM_011513724.1:c.3728+149_3728+151del	XP_011512026.1:n.3728+149_3728+151del
XM_011513725.1:c.3662+149_3662+151del	XP_011512027.1:n.3662+149_3662+151del
XM_011513726.1:c.3248+149_3248+151del	XP_011512028.1:n.3248+149_3248+151del
XM_011513727.1:c.3248+149_3248+151del	XP_011512029.1:n.3248+149_3248+151del
XM_011513728.1:c.3236+149_3236+151del	XP_011512030.1:n.3236+149_3236+151del
XR_925155.1:n.5426+149_5426+151del
NM_001317924.1:c.3236+149_3236+151del	NP_001304853.1:n.3236+149_3236+151del
XM_011513725.2:c.3662+149_3662+151del	XP_011512027.1:n.3662+149_3662+151del
XM_011513726.3:c.3248+149_3248+151del	XP_011512028.1:n.3248+149_3248+151del
XM_017008501.1:c.3236+149_3236+151del	XP_016863990.1:n.3236+149_3236+151del
XR_001741306.1:n.3792+149_3792+151del
XR_001741307.1:n.3780+149_3780+151del
XR_001741308.1:n.5426+149_5426+151del
XR_001741309.1:n.5414+149_5414+151del
XR_001741310.1:n.5414+149_5414+151del
XR_001741311.2:n.5263+149_5263+151del
NM_025132.4:c.3716+149_3716+151del MANE Select	NP_079408.3:n.3716+149_3716+151del
NM_001317924.2:c.3236+149_3236+151del	NP_001304853.1:n.3236+149_3236+151del