Canonical Allele Identifier: CA2743277407
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40080567_40080572del , CM000663.2:g.40080567_40080572del GRCh38
NC_000001.10:g.40546239_40546244del , CM000663.1:g.40546239_40546244del GRCh37
NC_000001.9:g.40318826_40318831del NCBI36
NG_009192.1:g.21899_21904del , LRG_690:g.21899_21904del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372779.9:c.*373-85_*373-80del ENSP00000361865.5:n.*373-85_*373-80del
ENST00000433473.8:c.534-85_534-80del ENSP00000394863.4:n.534-85_534-80del
ENST00000439754.6:c.537-85_537-80del ENSP00000403207.2:n.537-85_537-80del
ENST00000449045.7:c.228-85_228-80del ENSP00000392293.2:n.228-85_228-80del
ENST00000527311.7:c.306-85_306-80del ENSP00000436695.3:n.306-85_306-80del
ENST00000530076.6:c.-121-85_-121-80del ENSP00000434007.1:n.-121-85_-121-80del
ENST00000530704.6:c.*160-85_*160-80del ENSP00000431655.1:n.*160-85_*160-80del
ENST00000641083.1:c.515-85_515-80del
ENST00000641236.1:n.774-85_774-80del
ENST00000641319.1:c.537-85_537-80del ENSP00000493128.1:n.537-85_537-80del
ENST00000641381.1:c.149-3659_149-3654del
ENST00000641471.1:c.624-85_624-80del ENSP00000493146.1:n.624-85_624-80del
ENST00000641691.1:c.*389-85_*389-80del ENSP00000492910.1:n.*389-85_*389-80del
ENST00000641924.1:c.125-85_125-80del ENSP00000493063.1:n.125-85_125-80del
ENST00000642050.2:c.537-85_537-80del MANE Select ENSP00000493153.1:n.537-85_537-80del
ENST00000372779.8:c.624-85_624-80del ENSP00000361865.4:n.624-85_624-80del
ENST00000433473.7:c.537-85_537-80del ENSP00000394863.3:n.537-85_537-80del
ENST00000439754.5:c.222-85_222-80del ENSP00000403207.1:n.222-85_222-80del
ENST00000449045.6:c.228-85_228-80del ENSP00000392293.2:n.228-85_228-80del
ENST00000527311.6:c.312-85_312-80del ENSP00000436695.2:n.312-85_312-80del
ENST00000529905.5:c.537-85_537-80del ENSP00000432053.1:n.537-85_537-80del
ENST00000530076.5:c.-121-85_-121-80del ENSP00000434007.1:n.-121-85_-121-80del
ENST00000530704.5:c.*160-85_*160-80del ENSP00000431655.1:n.*160-85_*160-80del
NM_000310.3:c.537-85_537-80del , LRG_690t1:c.537-85_537-80del NP_000301.1:n.537-85_537-80del
NM_001142604.1:c.228-85_228-80del NP_001136076.1:n.228-85_228-80del
XM_005271008.1:c.537-85_537-80del XP_005271065.1:n.537-85_537-80del
NM_001363695.1:c.537-85_537-80del NP_001350624.1:n.537-85_537-80del
NM_000310.4:c.537-85_537-80del MANE Select NP_000301.1:n.537-85_537-80del
NM_001142604.2:c.228-85_228-80del NP_001136076.1:n.228-85_228-80del
NM_001363695.2:c.537-85_537-80del NP_001350624.1:n.537-85_537-80del