Canonical Allele Identifier: CA1164248593
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097254T= , CM000663.2:g.40097254T= GRCh38
NC_000001.10:g.40562926T= , CM000663.1:g.40562926T= GRCh37
NC_000001.9:g.40335513T= NCBI36
NG_009192.1:g.5217A= , LRG_690:g.5217A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000449045.7:c.-16A= ENSP00000392293.2:n.-16A=
ENST00000641319.1:c.-16A= ENSP00000493128.1:n.-16A=
ENST00000641691.1:c.-16A= ENSP00000492910.1:n.-16A=
ENST00000433473.7:c.-16A= ENSP00000394863.3:n.-16A=
NM_000310.3:c.-16A= , LRG_690t1:c.-16A= NP_000301.1:n.-16A=
NM_001142604.1:c.-16A= NP_001136076.1:n.-16A=
XM_005271008.1:c.-16A= XP_005271065.1:n.-16A=
NM_001363695.1:c.-16A= NP_001350624.1:n.-16A=