Canonical Allele Identifier: CA1164243684
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40074355_40074359delinsCTTTT , CM000663.2:g.40074355_40074359delinsCTTTT GRCh38
NC_000001.10:g.40540027_40540031delinsCTTTT , CM000663.1:g.40540027_40540031delinsCTTTT GRCh37
NC_000001.9:g.40312614_40312618delinsCTTTT NCBI36
NG_009192.1:g.28112_28116delinsAAAAG , LRG_690:g.28112_28116delinsAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.796-176_796-172delinsAAAAG ENSP00000394863.4:n.796-176_796-172delinsAAAAG
ENST00000439754.6:c.727-176_727-172delinsAAAAG ENSP00000403207.2:n.727-176_727-172delinsAAAAG
ENST00000449045.7:c.490-176_490-172delinsAAAAG ENSP00000392293.2:n.490-176_490-172delinsAAAAG
ENST00000527311.7:c.568-176_568-172delinsAAAAG ENSP00000436695.3:n.568-176_568-172delinsAAAAG
ENST00000530076.6:c.142-176_142-172delinsAAAAG ENSP00000434007.1:n.142-176_142-172delinsAAAAG
ENST00000530704.6:c.*422-176_*422-172delinsAAAAG ENSP00000431655.1:n.*422-176_*422-172delinsAAAAG
ENST00000641083.1:c.889-176_889-172delinsAAAAG
ENST00000641236.1:n.1036-176_1036-172delinsAAAAG
ENST00000641319.1:c.*9-176_*9-172delinsAAAAG ENSP00000493128.1:n.*9-176_*9-172delinsAAAAG
ENST00000641381.1:c.221-176_221-172delinsAAAAG
ENST00000641471.1:c.886-176_886-172delinsAAAAG ENSP00000493146.1:n.886-176_886-172delinsAAAAG
ENST00000641691.1:c.*651-176_*651-172delinsAAAAG ENSP00000492910.1:n.*651-176_*651-172delinsAAAAG
ENST00000641924.1:c.*228-176_*228-172delinsAAAAG ENSP00000493063.1:n.*228-176_*228-172delinsAAAAG
ENST00000642050.2:c.799-176_799-172delinsAAAAG MANE Select ENSP00000493153.1:n.799-176_799-172delinsAAAAG
ENST00000372775.2:n.196-176_196-172delinsAAAAG
ENST00000433473.7:c.799-176_799-172delinsAAAAG ENSP00000394863.3:n.799-176_799-172delinsAAAAG
ENST00000439754.5:c.412-176_412-172delinsAAAAG ENSP00000403207.1:n.412-176_412-172delinsAAAAG
ENST00000449045.6:c.490-176_490-172delinsAAAAG ENSP00000392293.2:n.490-176_490-172delinsAAAAG
ENST00000527311.6:c.574-176_574-172delinsAAAAG ENSP00000436695.2:n.574-176_574-172delinsAAAAG
ENST00000529905.5:c.799-176_799-172delinsAAAAG ENSP00000432053.1:n.799-176_799-172delinsAAAAG
ENST00000530076.5:c.142-176_142-172delinsAAAAG ENSP00000434007.1:n.142-176_142-172delinsAAAAG
ENST00000530704.5:c.*422-176_*422-172delinsAAAAG ENSP00000431655.1:n.*422-176_*422-172delinsAAAAG
NM_000310.3:c.799-176_799-172delinsAAAAG , LRG_690t1:c.799-176_799-172delinsAAAAG NP_000301.1:n.799-176_799-172delinsAAAAG
NM_001142604.1:c.490-176_490-172delinsAAAAG NP_001136076.1:n.490-176_490-172delinsAAAAG
XM_005271008.1:c.727-176_727-172delinsAAAAG XP_005271065.1:n.727-176_727-172delinsAAAAG
NM_001363695.1:c.727-176_727-172delinsAAAAG NP_001350624.1:n.727-176_727-172delinsAAAAG
NM_000310.4:c.799-176_799-172delinsAAAAG MANE Select NP_000301.1:n.799-176_799-172delinsAAAAG
NM_001142604.2:c.490-176_490-172delinsAAAAG NP_001136076.1:n.490-176_490-172delinsAAAAG
NM_001363695.2:c.727-176_727-172delinsAAAAG NP_001350624.1:n.727-176_727-172delinsAAAAG