Canonical Allele Identifier: CA735683445

Gene: PPT1

Linked Data

• dbSNP Id: rs763337954
• gnomAD v3: 1-40074027-G-C
• gnomAD v4: 1-40074027-G-C
• MyVariant Identifiers: chr1:g.40539699G>C (hg19) ; chr1:g.40074027G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074027G>C , CM000663.2:g.40074027G>C	GRCh38
NC_000001.10:g.40539699G>C , CM000663.1:g.40539699G>C	GRCh37
NC_000001.9:g.40312286G>C	NCBI36
NG_009192.1:g.28444C>G , LRG_690:g.28444C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.*34C>G	ENSP00000394863.4:n.*34C>G
ENST00000439754.6:c.*34C>G	ENSP00000403207.2:n.*34C>G
ENST00000449045.7:c.*34C>G	ENSP00000392293.2:n.*34C>G
ENST00000530076.6:c.*34C>G	ENSP00000434007.1:n.*34C>G
ENST00000530704.6:c.*578C>G	ENSP00000431655.1:n.*578C>G
ENST00000641083.1:c.1045C>G
ENST00000641236.1:n.1192C>G
ENST00000641319.1:c.*165C>G	ENSP00000493128.1:n.*165C>G
ENST00000641381.1:c.377C>G
ENST00000641471.1:c.*34C>G	ENSP00000493146.1:n.*34C>G
ENST00000641691.1:c.*807C>G	ENSP00000492910.1:n.*807C>G
ENST00000641924.1:c.*384C>G	ENSP00000493063.1:n.*384C>G
ENST00000642050.2:c.*34C>G MANE Select	ENSP00000493153.1:n.*34C>G
ENST00000372775.2:n.352C>G
ENST00000433473.7:c.*34C>G	ENSP00000394863.3:n.*34C>G
ENST00000439754.5:c.568C>G	ENSP00000403207.1:n.568C>G
ENST00000449045.6:c.*34C>G	ENSP00000392293.2:n.*34C>G
ENST00000529905.5:c.*34C>G	ENSP00000432053.1:n.*34C>G
ENST00000530704.5:c.*578C>G	ENSP00000431655.1:n.*578C>G
NM_000310.3:c.*34C>G , LRG_690t1:c.*34C>G	NP_000301.1:n.*34C>G
NM_001142604.1:c.*34C>G	NP_001136076.1:n.*34C>G
XM_005271008.1:c.*34C>G	XP_005271065.1:n.*34C>G
NM_001363695.1:c.*34C>G	NP_001350624.1:n.*34C>G
NM_000310.4:c.*34C>G MANE Select	NP_000301.1:n.*34C>G
NM_001142604.2:c.*34C>G	NP_001136076.1:n.*34C>G
NM_001363695.2:c.*34C>G	NP_001350624.1:n.*34C>G