Canonical Allele Identifier: CA21021494
Gene: PPT1 HGNC NCBI

Linked Data

dbSNP Id: rs559058511
gnomAD v3: 1-40097311-C-T
gnomAD v4: 1-40097311-C-T

Genomic Alleles

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

Transcript Alleles

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