Canonical Allele Identifier: CA339847673

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40546099G>C (hg19) ; chr1:g.40080427G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40080427G>C , CM000663.2:g.40080427G>C	GRCh38
NC_000001.10:g.40546099G>C , CM000663.1:g.40546099G>C	GRCh37
NC_000001.9:g.40318686G>C	NCBI36
NG_009192.1:g.22044C>G , LRG_690:g.22044C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.594C>G	ENSP00000394863.4:p.Ser198Arg
ENST00000439754.6:c.597C>G	ENSP00000403207.2:p.Ser199Arg
ENST00000449045.7:c.288C>G	ENSP00000392293.2:p.Ser96Arg
ENST00000527311.7:c.366C>G	ENSP00000436695.3:p.Ser122Arg
ENST00000530076.6:c.-61C>G	ENSP00000434007.1:n.-61C>G
ENST00000530704.6:c.*220C>G	ENSP00000431655.1:n.*220C>G
ENST00000641083.1:c.575C>G
ENST00000641236.1:n.834C>G
ENST00000641319.1:c.597C>G	ENSP00000493128.1:p.Ser199Arg
ENST00000641381.1:c.149-3514C>G
ENST00000641471.1:c.684C>G	ENSP00000493146.1:p.Ser228Arg
ENST00000641691.1:c.*449C>G	ENSP00000492910.1:n.*449C>G
ENST00000641924.1:c.*26C>G	ENSP00000493063.1:n.*26C>G
ENST00000642050.2:c.597C>G MANE Select	ENSP00000493153.1:p.Ser199Arg
ENST00000372779.8:c.684C>G	ENSP00000361865.4:p.Ser228Arg
ENST00000433473.7:c.597C>G	ENSP00000394863.3:p.Ser199Arg
ENST00000439754.5:c.282C>G	ENSP00000403207.1:p.Ser94Arg
ENST00000449045.6:c.288C>G	ENSP00000392293.2:p.Ser96Arg
ENST00000527311.6:c.372C>G	ENSP00000436695.2:p.Ser124Arg
ENST00000529905.5:c.597C>G	ENSP00000432053.1:p.Ser199Arg
ENST00000530076.5:c.-61C>G	ENSP00000434007.1:n.-61C>G
ENST00000530704.5:c.*220C>G	ENSP00000431655.1:n.*220C>G
NM_000310.3:c.597C>G , LRG_690t1:c.597C>G	NP_000301.1:p.Ser199Arg
NM_001142604.1:c.288C>G	NP_001136076.1:p.Ser96Arg
XM_005271008.1:c.597C>G	XP_005271065.1:p.Ser199Arg
NM_001363695.1:c.597C>G	NP_001350624.1:p.Ser199Arg
NM_000310.4:c.597C>G MANE Select	NP_000301.1:p.Ser199Arg
NM_001142604.2:c.288C>G	NP_001136076.1:p.Ser96Arg
NM_001363695.2:c.597C>G	NP_001350624.1:p.Ser199Arg