Canonical Allele Identifier: CA339846978

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40544327T>C (hg19) ; chr1:g.40078655T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40078655T>C , CM000663.2:g.40078655T>C	GRCh38
NC_000001.10:g.40544327T>C , CM000663.1:g.40544327T>C	GRCh37
NC_000001.9:g.40316914T>C	NCBI36
NG_009192.1:g.23816A>G , LRG_690:g.23816A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.628A>G	ENSP00000394863.4:p.Ile210Val
ENST00000439754.6:c.631A>G	ENSP00000403207.2:p.Ile211Val
ENST00000449045.7:c.322A>G	ENSP00000392293.2:p.Ile108Val
ENST00000527311.7:c.400A>G	ENSP00000436695.3:p.Ile134Val
ENST00000530076.6:c.-27A>G	ENSP00000434007.1:n.-27A>G
ENST00000530704.6:c.*254A>G	ENSP00000431655.1:n.*254A>G
ENST00000641083.1:c.609A>G
ENST00000641236.1:n.868A>G
ENST00000641319.1:c.631A>G	ENSP00000493128.1:p.Ile211Val
ENST00000641381.1:c.149-1742A>G
ENST00000641471.1:c.718A>G	ENSP00000493146.1:p.Ile240Val
ENST00000641691.1:c.*483A>G	ENSP00000492910.1:n.*483A>G
ENST00000641924.1:c.*60A>G	ENSP00000493063.1:n.*60A>G
ENST00000642050.2:c.631A>G MANE Select	ENSP00000493153.1:p.Ile211Val
ENST00000372775.2:n.28A>G
ENST00000372779.8:c.718A>G	ENSP00000361865.4:p.Ile240Val
ENST00000433473.7:c.631A>G	ENSP00000394863.3:p.Ile211Val
ENST00000439754.5:c.316A>G	ENSP00000403207.1:p.Ile106Val
ENST00000449045.6:c.322A>G	ENSP00000392293.2:p.Ile108Val
ENST00000527311.6:c.406A>G	ENSP00000436695.2:p.Ile136Val
ENST00000529905.5:c.631A>G	ENSP00000432053.1:p.Ile211Val
ENST00000530076.5:c.-27A>G	ENSP00000434007.1:n.-27A>G
ENST00000530704.5:c.*254A>G	ENSP00000431655.1:n.*254A>G
NM_000310.3:c.631A>G , LRG_690t1:c.631A>G	NP_000301.1:p.Ile211Val
NM_001142604.1:c.322A>G	NP_001136076.1:p.Ile108Val
XM_005271008.1:c.631A>G	XP_005271065.1:p.Ile211Val
NM_001363695.1:c.631A>G	NP_001350624.1:p.Ile211Val
NM_000310.4:c.631A>G MANE Select	NP_000301.1:p.Ile211Val
NM_001142604.2:c.322A>G	NP_001136076.1:p.Ile108Val
NM_001363695.2:c.631A>G	NP_001350624.1:p.Ile211Val