Canonical Allele Identifier: CA1164248727
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097348C= , CM000663.2:g.40097348C= GRCh38
NC_000001.10:g.40563020C= , CM000663.1:g.40563020C= GRCh37
NC_000001.9:g.40335607C= NCBI36
NG_009192.1:g.5123G= , LRG_690:g.5123G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-110G= ENSP00000394863.3:n.-110G=
NM_000310.3:c.-110G= , LRG_690t1:c.-110G= NP_000301.1:n.-110G=
NM_001142604.1:c.-110G= NP_001136076.1:n.-110G=
NM_001363695.1:c.-110G= NP_001350624.1:n.-110G=