Canonical Allele Identifier: CA1164248627
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097281C= , CM000663.2:g.40097281C= GRCh38
NC_000001.10:g.40562953C= , CM000663.1:g.40562953C= GRCh37
NC_000001.9:g.40335540C= NCBI36
NG_009192.1:g.5190G= , LRG_690:g.5190G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-43G= ENSP00000394863.3:n.-43G=
NM_000310.3:c.-43G= , LRG_690t1:c.-43G= NP_000301.1:n.-43G=
NM_001142604.1:c.-43G= NP_001136076.1:n.-43G=
NM_001363695.1:c.-43G= NP_001350624.1:n.-43G=