Canonical Allele Identifier: CA339849972

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40558138T>C (hg19) ; chr1:g.40092466T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092466T>C , CM000663.2:g.40092466T>C	GRCh38
NC_000001.10:g.40558138T>C , CM000663.1:g.40558138T>C	GRCh37
NC_000001.9:g.40330725T>C	NCBI36
NG_009192.1:g.10005A>G , LRG_690:g.10005A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*2A>G	ENSP00000361865.5:n.*2A>G
ENST00000433473.8:c.163A>G	ENSP00000394863.4:p.Lys55Glu
ENST00000439754.6:c.166A>G	ENSP00000403207.2:p.Lys56Glu
ENST00000449045.7:c.125-2954A>G	ENSP00000392293.2:n.125-2954A>G
ENST00000526547.2:c.446A>G
ENST00000527311.7:c.166A>G	ENSP00000436695.3:p.Lys56Glu
ENST00000530704.6:c.166A>G	ENSP00000431655.1:p.Lys56Glu
ENST00000641083.1:c.144A>G
ENST00000641236.1:n.178A>G
ENST00000641319.1:c.166A>G	ENSP00000493128.1:p.Lys56Glu
ENST00000641471.1:c.253A>G	ENSP00000493146.1:p.Lys85Glu
ENST00000641548.1:c.*18A>G	ENSP00000492984.1:n.*18A>G
ENST00000641691.1:c.*18A>G	ENSP00000492910.1:n.*18A>G
ENST00000641924.1:c.124+4649A>G	ENSP00000493063.1:n.124+4649A>G
ENST00000642050.2:c.166A>G MANE Select	ENSP00000493153.1:p.Lys56Glu
ENST00000372779.8:c.253A>G	ENSP00000361865.4:p.Lys85Glu
ENST00000433473.7:c.166A>G	ENSP00000394863.3:p.Lys56Glu
ENST00000449045.6:c.125-2954A>G	ENSP00000392293.2:n.125-2954A>G
ENST00000526547.1:c.16A>G	ENSP00000436481.1:p.Lys6Glu
ENST00000527311.6:c.125-409A>G	ENSP00000436695.2:n.125-409A>G
ENST00000529905.5:c.166A>G	ENSP00000432053.1:p.Lys56Glu
ENST00000530704.5:c.166A>G	ENSP00000431655.1:p.Lys56Glu
NM_000310.3:c.166A>G , LRG_690t1:c.166A>G	NP_000301.1:p.Lys56Glu
NM_001142604.1:c.125-2954A>G	NP_001136076.1:n.125-2954A>G
XM_005271008.1:c.166A>G	XP_005271065.1:p.Lys56Glu
NM_001363695.1:c.166A>G	NP_001350624.1:p.Lys56Glu
NM_000310.4:c.166A>G MANE Select	NP_000301.1:p.Lys56Glu
NM_001142604.2:c.125-2954A>G	NP_001136076.1:n.125-2954A>G
NM_001363695.2:c.166A>G	NP_001350624.1:p.Lys56Glu