Canonical Allele Identifier: CA1164248751
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097389G= , CM000663.2:g.40097389G= GRCh38
NC_000001.10:g.40563061G= , CM000663.1:g.40563061G= GRCh37
NC_000001.9:g.40335648G= NCBI36
NG_009192.1:g.5082C= , LRG_690:g.5082C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-151C= ENSP00000394863.3:n.-151C=
NM_000310.3:c.-151C= , LRG_690t1:c.-151C= NP_000301.1:n.-151C=
NM_001142604.1:c.-151C= NP_001136076.1:n.-151C=
NM_001363695.1:c.-151C= NP_001350624.1:n.-151C=