Canonical Allele Identifier: CA2839797691

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40073980C>A , CM000663.2:g.40073980C>A	GRCh38
NC_000001.10:g.40539652C>A , CM000663.1:g.40539652C>A	GRCh37
NC_000001.9:g.40312239C>A	NCBI36
NG_009192.1:g.28491G>T , LRG_690:g.28491G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.*81G>T	ENSP00000394863.4:n.*81G>T
ENST00000439754.6:c.*81G>T	ENSP00000403207.2:n.*81G>T
ENST00000449045.7:c.*81G>T	ENSP00000392293.2:n.*81G>T
ENST00000530076.6:c.*81G>T	ENSP00000434007.1:n.*81G>T
ENST00000530704.6:c.*625G>T	ENSP00000431655.1:n.*625G>T
ENST00000641083.1:c.1092G>T
ENST00000641236.1:n.1239G>T
ENST00000641319.1:c.*212G>T	ENSP00000493128.1:n.*212G>T
ENST00000641381.1:c.424G>T
ENST00000641471.1:c.*81G>T	ENSP00000493146.1:n.*81G>T
ENST00000641691.1:c.*854G>T	ENSP00000492910.1:n.*854G>T
ENST00000642050.2:c.*81G>T MANE Select	ENSP00000493153.1:n.*81G>T
ENST00000372775.2:n.399G>T
ENST00000433473.7:c.*81G>T	ENSP00000394863.3:n.*81G>T
ENST00000439754.5:c.615G>T	ENSP00000403207.1:n.615G>T
ENST00000449045.6:c.*81G>T	ENSP00000392293.2:n.*81G>T
ENST00000529905.5:c.*81G>T	ENSP00000432053.1:n.*81G>T
ENST00000530704.5:c.*625G>T	ENSP00000431655.1:n.*625G>T
NM_000310.3:c.*81G>T , LRG_690t1:c.*81G>T	NP_000301.1:n.*81G>T
NM_001142604.1:c.*81G>T	NP_001136076.1:n.*81G>T
XM_005271008.1:c.*81G>T	XP_005271065.1:n.*81G>T
NM_001363695.1:c.*81G>T	NP_001350624.1:n.*81G>T
NM_000310.4:c.*81G>T MANE Select	NP_000301.1:n.*81G>T
NM_001142604.2:c.*81G>T	NP_001136076.1:n.*81G>T
NM_001363695.2:c.*81G>T	NP_001350624.1:n.*81G>T