Canonical Allele Identifier: CA1146657835
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097311C= , CM000663.2:g.40097311C= GRCh38
NC_000001.10:g.40562983C= , CM000663.1:g.40562983C= GRCh37
NC_000001.9:g.40335570C= NCBI36
NG_009192.1:g.5160G= , LRG_690:g.5160G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-73G= ENSP00000394863.3:n.-73G=
NM_000310.3:c.-73G= , LRG_690t1:c.-73G= NP_000301.1:n.-73G=
NM_001142604.1:c.-73G= NP_001136076.1:n.-73G=
NM_001363695.1:c.-73G= NP_001350624.1:n.-73G=