Canonical Allele Identifier: CA339845610

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40539806A>G (hg19) ; chr1:g.40074134A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074134A>G , CM000663.2:g.40074134A>G	GRCh38
NC_000001.10:g.40539806A>G , CM000663.1:g.40539806A>G	GRCh37
NC_000001.9:g.40312393A>G	NCBI36
NG_009192.1:g.28337T>C , LRG_690:g.28337T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.845T>C	ENSP00000394863.4:p.Leu282Pro
ENST00000439754.6:c.776T>C	ENSP00000403207.2:p.Leu259Pro
ENST00000449045.7:c.539T>C	ENSP00000392293.2:p.Leu180Pro
ENST00000527311.7:c.617T>C	ENSP00000436695.3:p.Leu206Pro
ENST00000530076.6:c.191T>C	ENSP00000434007.1:p.Leu64Pro
ENST00000530704.6:c.*471T>C	ENSP00000431655.1:n.*471T>C
ENST00000641083.1:c.938T>C
ENST00000641236.1:n.1085T>C
ENST00000641319.1:c.*58T>C	ENSP00000493128.1:n.*58T>C
ENST00000641381.1:c.270T>C
ENST00000641471.1:c.935T>C	ENSP00000493146.1:p.Leu312Pro
ENST00000641691.1:c.*700T>C	ENSP00000492910.1:n.*700T>C
ENST00000641924.1:c.*277T>C	ENSP00000493063.1:n.*277T>C
ENST00000642050.2:c.848T>C MANE Select	ENSP00000493153.1:p.Leu283Pro
ENST00000372775.2:n.245T>C
ENST00000433473.7:c.848T>C	ENSP00000394863.3:p.Leu283Pro
ENST00000439754.5:c.461T>C	ENSP00000403207.1:p.Leu154Pro
ENST00000449045.6:c.539T>C	ENSP00000392293.2:p.Leu180Pro
ENST00000529905.5:c.848T>C	ENSP00000432053.1:p.Leu283Pro
ENST00000530076.5:c.191T>C	ENSP00000434007.1:p.Leu64Pro
ENST00000530704.5:c.*471T>C	ENSP00000431655.1:n.*471T>C
NM_000310.3:c.848T>C , LRG_690t1:c.848T>C	NP_000301.1:p.Leu283Pro
NM_001142604.1:c.539T>C	NP_001136076.1:p.Leu180Pro
XM_005271008.1:c.776T>C	XP_005271065.1:p.Leu259Pro
NM_001363695.1:c.776T>C	NP_001350624.1:p.Leu259Pro
NM_000310.4:c.848T>C MANE Select	NP_000301.1:p.Leu283Pro
NM_001142604.2:c.539T>C	NP_001136076.1:p.Leu180Pro
NM_001363695.2:c.776T>C	NP_001350624.1:p.Leu259Pro