Canonical Allele Identifier: CA417322777

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557755G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092083G>C , CM000663.2:g.40092083G>C	GRCh38
NC_000001.10:g.40557755G>C , CM000663.1:g.40557755G>C	GRCh37
NC_000001.9:g.40330342G>C	NCBI36
NG_009192.1:g.10388C>G , LRG_690:g.10388C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*160C>G	ENSP00000361865.5:n.*160C>G
ENST00000433473.8:c.321C>G	ENSP00000394863.4:p.Gly107=
ENST00000439754.6:c.324C>G	ENSP00000403207.2:p.Gly108=
ENST00000449045.7:c.125-2571C>G	ENSP00000392293.2:n.125-2571C>G
ENST00000526547.2:c.604C>G
ENST00000527311.7:c.234+315C>G	ENSP00000436695.3:n.234+315C>G
ENST00000530704.6:c.324C>G	ENSP00000431655.1:p.Gly108=
ENST00000641083.1:c.302C>G
ENST00000641236.1:n.561C>G
ENST00000641319.1:c.324C>G	ENSP00000493128.1:p.Gly108=
ENST00000641471.1:c.411C>G	ENSP00000493146.1:p.Gly137=
ENST00000641548.1:c.*176C>G	ENSP00000492984.1:n.*176C>G
ENST00000641691.1:c.*176C>G	ENSP00000492910.1:n.*176C>G
ENST00000641924.1:c.124+5032C>G	ENSP00000493063.1:n.124+5032C>G
ENST00000642050.2:c.324C>G MANE Select	ENSP00000493153.1:p.Gly108=
ENST00000372779.8:c.411C>G	ENSP00000361865.4:p.Gly137=
ENST00000433473.7:c.324C>G	ENSP00000394863.3:p.Gly108=
ENST00000439754.5:c.9C>G	ENSP00000403207.1:p.Gly3=
ENST00000449045.6:c.125-2571C>G	ENSP00000392293.2:n.125-2571C>G
ENST00000526547.1:c.174C>G	ENSP00000436481.1:p.Gly58=
ENST00000527311.6:c.125-26C>G	ENSP00000436695.2:n.125-26C>G
ENST00000529905.5:c.324C>G	ENSP00000432053.1:p.Gly108=
ENST00000530704.5:c.324C>G	ENSP00000431655.1:p.Gly108=
NM_000310.3:c.324C>G , LRG_690t1:c.324C>G	NP_000301.1:p.Gly108=
NM_001142604.1:c.125-2571C>G	NP_001136076.1:n.125-2571C>G
XM_005271008.1:c.324C>G	XP_005271065.1:p.Gly108=
NM_001363695.1:c.324C>G	NP_001350624.1:p.Gly108=
NM_000310.4:c.324C>G MANE Select	NP_000301.1:p.Gly108=
NM_001142604.2:c.125-2571C>G	NP_001136076.1:n.125-2571C>G
NM_001363695.2:c.324C>G	NP_001350624.1:p.Gly108=