Canonical Allele Identifier: CA916083330
Community Standard Title: NM_032147.5(USP44):c.873_886delinsT (p.Leu291PhefsTer8)
Gene: USP44 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95533371_95533384delinsA , CM000674.2:g.95533371_95533384delinsA GRCh38
NC_000012.11:g.95927147_95927160delinsA , CM000674.1:g.95927147_95927160delinsA GRCh37
NC_000012.10:g.94451278_94451291delinsA NCBI36
NG_052622.1:g.23146_23159delinsT

Transcript Alleles

HGVS Amino-acid Change
NM_032147.5:c.873_886delinsT MANE Select NP_115523.2:p.Leu291PhefsTer8
ENST00000258499.8:c.873_886delinsT MANE Select ENSP00000258499.3:p.Leu291PhefsTer8
NM_001042403.2:c.873_886delinsT NP_001035862.1:p.Leu291PhefsTer8
NM_001042403.3:c.873_886delinsT NP_001035862.1:p.Leu291PhefsTer8
NM_001278393.1:c.873_886delinsT NP_001265322.1:p.Leu291PhefsTer8
NM_001278393.2:c.873_886delinsT NP_001265322.1:p.Leu291PhefsTer8
NM_001347936.1:c.873_886delinsT NP_001334865.1:p.Leu291PhefsTer8
NM_001347936.2:c.873_886delinsT NP_001334865.1:p.Leu291PhefsTer8
NM_001347937.1:c.873_886delinsT NP_001334866.1:p.Leu291PhefsTer8
NM_001347937.2:c.873_886delinsT NP_001334866.1:p.Leu291PhefsTer8
NM_032147.4:c.873_886delinsT NP_115523.2:p.Leu291PhefsTer8
NR_125360.1:n.943_956delinsT
NR_125360.2:n.1071_1084delinsT
NR_125360.3:n.1029_1042delinsT
NR_144944.1:n.1262_1275delinsT
NR_144944.2:n.1220_1233delinsT
NR_144945.1:n.1017_1030delinsT
NR_144945.2:n.975_988delinsT
NR_144946.1:n.1017_1030delinsT
NR_144946.2:n.975_988delinsT
NR_144947.1:n.1017_1030delinsT
NR_144947.2:n.975_988delinsT
NR_144948.1:n.1262_1275delinsT
NR_144948.2:n.1220_1233delinsT
ENST00000258499.7:c.873_886delinsT ENSP00000258499.3:p.Leu291PhefsTer8
ENST00000393091.6:c.873_886delinsT ENSP00000376806.2:p.Leu291PhefsTer8
ENST00000537435.2:c.873_886delinsT ENSP00000442629.2:p.Leu291PhefsTer8
ENST00000552440.5:c.873_886delinsT ENSP00000448670.1:p.Leu291PhefsTer8
XM_005269172.1:c.873_886delinsT XP_005269229.1:p.Leu291PhefsTer8
XM_005269173.1:c.873_886delinsT XP_005269230.1:p.Leu291PhefsTer8
XM_005269174.1:c.873_886delinsT XP_005269231.1:p.Leu291PhefsTer8
XM_006719628.1:c.873_886delinsT XP_006719691.1:p.Leu291PhefsTer8
XM_011538800.1:c.873_886delinsT XP_011537102.1:p.Leu291PhefsTer8
XM_011538800.2:c.873_886delinsT XP_011537102.1:p.Leu291PhefsTer8
XM_011538801.1:c.873_886delinsT XP_011537103.1:p.Leu291PhefsTer8
XM_011538802.1:c.873_886delinsT XP_011537104.1:p.Leu291PhefsTer8
XM_011538803.1:c.873_886delinsT XP_011537105.1:p.Leu291PhefsTer8
XM_011538804.1:c.873_886delinsT XP_011537106.1:p.Leu291PhefsTer8
XM_011538804.2:c.873_886delinsT XP_011537106.1:p.Leu291PhefsTer8
XM_011538805.1:c.873_886delinsT XP_011537107.1:p.Leu291PhefsTer8
XM_011538805.2:c.873_886delinsT XP_011537107.1:p.Leu291PhefsTer8
XM_011538806.1:c.873_886delinsT XP_011537108.1:p.Leu291PhefsTer8
XM_011538806.2:c.873_886delinsT XP_011537108.1:p.Leu291PhefsTer8
XM_017020010.2:c.873_886delinsT XP_016875499.1:p.Leu291PhefsTer8
XM_017020012.1:c.873_886delinsT XP_016875501.1:p.Leu291PhefsTer8
XR_001748887.1:n.1156_1169delinsT
XR_944757.1:n.1156_1169delinsT
XR_944758.1:n.1234_1247delinsT