Canonical Allele Identifier: CA339846907

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40544313G>T (hg19) ; chr1:g.40078641G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40078641G>T , CM000663.2:g.40078641G>T	GRCh38
NC_000001.10:g.40544313G>T , CM000663.1:g.40544313G>T	GRCh37
NC_000001.9:g.40316900G>T	NCBI36
NG_009192.1:g.23830C>A , LRG_690:g.23830C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000433473.8:c.642C>A	ENSP00000394863.4:p.Tyr214Ter
ENST00000439754.6:c.645C>A	ENSP00000403207.2:p.Tyr215Ter
ENST00000449045.7:c.336C>A	ENSP00000392293.2:p.Tyr112Ter
ENST00000527311.7:c.414C>A	ENSP00000436695.3:p.Tyr138Ter
ENST00000530076.6:c.-13C>A	ENSP00000434007.1:n.-13C>A
ENST00000530704.6:c.*268C>A	ENSP00000431655.1:n.*268C>A
ENST00000641083.1:c.623C>A
ENST00000641236.1:n.882C>A
ENST00000641319.1:c.645C>A	ENSP00000493128.1:p.Tyr215Ter
ENST00000641381.1:c.149-1728C>A
ENST00000641471.1:c.732C>A	ENSP00000493146.1:p.Tyr244Ter
ENST00000641691.1:c.*497C>A	ENSP00000492910.1:n.*497C>A
ENST00000641924.1:c.*74C>A	ENSP00000493063.1:n.*74C>A
ENST00000642050.2:c.645C>A MANE Select	ENSP00000493153.1:p.Tyr215Ter
ENST00000372775.2:n.42C>A
ENST00000372779.8:c.732C>A	ENSP00000361865.4:p.Tyr244Ter
ENST00000433473.7:c.645C>A	ENSP00000394863.3:p.Tyr215Ter
ENST00000439754.5:c.330C>A	ENSP00000403207.1:p.Tyr110Ter
ENST00000449045.6:c.336C>A	ENSP00000392293.2:p.Tyr112Ter
ENST00000527311.6:c.420C>A	ENSP00000436695.2:p.Tyr140Ter
ENST00000529905.5:c.645C>A	ENSP00000432053.1:p.Tyr215Ter
ENST00000530076.5:c.-13C>A	ENSP00000434007.1:n.-13C>A
ENST00000530704.5:c.*268C>A	ENSP00000431655.1:n.*268C>A
NM_000310.3:c.645C>A , LRG_690t1:c.645C>A	NP_000301.1:p.Tyr215Ter
NM_001142604.1:c.336C>A	NP_001136076.1:p.Tyr112Ter
XM_005271008.1:c.645C>A	XP_005271065.1:p.Tyr215Ter
NM_001363695.1:c.645C>A	NP_001350624.1:p.Tyr215Ter
NM_000310.4:c.645C>A MANE Select	NP_000301.1:p.Tyr215Ter
NM_001142604.2:c.336C>A	NP_001136076.1:p.Tyr112Ter
NM_001363695.2:c.645C>A	NP_001350624.1:p.Tyr215Ter