Canonical Allele Identifier: CA21021529
Gene: PPT1 HGNC NCBI

Linked Data

dbSNP Id: rs768166471
gnomAD v3: 1-40097328-C-T
gnomAD v4: 1-40097328-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097328C>T , CM000663.2:g.40097328C>T GRCh38
NC_000001.10:g.40563000C>T , CM000663.1:g.40563000C>T GRCh37
NC_000001.9:g.40335587C>T NCBI36
NG_009192.1:g.5143G>A , LRG_690:g.5143G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-90G>A ENSP00000394863.3:n.-90G>A
NM_000310.3:c.-90G>A , LRG_690t1:c.-90G>A NP_000301.1:n.-90G>A
NM_001142604.1:c.-90G>A NP_001136076.1:n.-90G>A
NM_001363695.1:c.-90G>A NP_001350624.1:n.-90G>A