Canonical Allele Identifier: CA339849597

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40558083T>C (hg19) ; chr1:g.40092411T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092411T>C , CM000663.2:g.40092411T>C	GRCh38
NC_000001.10:g.40558083T>C , CM000663.1:g.40558083T>C	GRCh37
NC_000001.9:g.40330670T>C	NCBI36
NG_009192.1:g.10060A>G , LRG_690:g.10060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*57A>G	ENSP00000361865.5:n.*57A>G
ENST00000433473.8:c.218A>G	ENSP00000394863.4:p.Lys73Arg
ENST00000439754.6:c.221A>G	ENSP00000403207.2:p.Lys74Arg
ENST00000449045.7:c.125-2899A>G	ENSP00000392293.2:n.125-2899A>G
ENST00000526547.2:c.501A>G
ENST00000527311.7:c.221A>G	ENSP00000436695.3:p.Lys74Arg
ENST00000530704.6:c.221A>G	ENSP00000431655.1:p.Lys74Arg
ENST00000641083.1:c.199A>G
ENST00000641236.1:n.233A>G
ENST00000641319.1:c.221A>G	ENSP00000493128.1:p.Lys74Arg
ENST00000641471.1:c.308A>G	ENSP00000493146.1:p.Lys103Arg
ENST00000641548.1:c.*73A>G	ENSP00000492984.1:n.*73A>G
ENST00000641691.1:c.*73A>G	ENSP00000492910.1:n.*73A>G
ENST00000641924.1:c.124+4704A>G	ENSP00000493063.1:n.124+4704A>G
ENST00000642050.2:c.221A>G MANE Select	ENSP00000493153.1:p.Lys74Arg
ENST00000372779.8:c.308A>G	ENSP00000361865.4:p.Lys103Arg
ENST00000433473.7:c.221A>G	ENSP00000394863.3:p.Lys74Arg
ENST00000449045.6:c.125-2899A>G	ENSP00000392293.2:n.125-2899A>G
ENST00000526547.1:c.71A>G	ENSP00000436481.1:p.Lys24Arg
ENST00000527311.6:c.125-354A>G	ENSP00000436695.2:n.125-354A>G
ENST00000529905.5:c.221A>G	ENSP00000432053.1:p.Lys74Arg
ENST00000530704.5:c.221A>G	ENSP00000431655.1:p.Lys74Arg
NM_000310.3:c.221A>G , LRG_690t1:c.221A>G	NP_000301.1:p.Lys74Arg
NM_001142604.1:c.125-2899A>G	NP_001136076.1:n.125-2899A>G
XM_005271008.1:c.221A>G	XP_005271065.1:p.Lys74Arg
NM_001363695.1:c.221A>G	NP_001350624.1:p.Lys74Arg
NM_000310.4:c.221A>G MANE Select	NP_000301.1:p.Lys74Arg
NM_001142604.2:c.125-2899A>G	NP_001136076.1:n.125-2899A>G
NM_001363695.2:c.221A>G	NP_001350624.1:p.Lys74Arg