Canonical Allele Identifier: CA735683954

Gene: PPT1

Linked Data

• dbSNP Id: rs1410453350
• MyVariant Identifiers: chr1:g.40540039_40540048del (hg19) ; chr1:g.40074367_40074376del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074375_40074384del , CM000663.2:g.40074375_40074384del	GRCh38
NC_000001.10:g.40540047_40540056del , CM000663.1:g.40540047_40540056del	GRCh37
NC_000001.9:g.40312634_40312643del	NCBI36
NG_009192.1:g.28095_28104del , LRG_690:g.28095_28104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.796-193_796-184del	ENSP00000394863.4:n.796-193_796-184del
ENST00000439754.6:c.727-193_727-184del	ENSP00000403207.2:n.727-193_727-184del
ENST00000449045.7:c.490-193_490-184del	ENSP00000392293.2:n.490-193_490-184del
ENST00000527311.7:c.568-193_568-184del	ENSP00000436695.3:n.568-193_568-184del
ENST00000530076.6:c.142-193_142-184del	ENSP00000434007.1:n.142-193_142-184del
ENST00000530704.6:c.*422-193_*422-184del	ENSP00000431655.1:n.*422-193_*422-184del
ENST00000641083.1:c.889-193_889-184del
ENST00000641236.1:n.1036-193_1036-184del
ENST00000641319.1:c.*9-193_*9-184del	ENSP00000493128.1:n.*9-193_*9-184del
ENST00000641381.1:c.221-193_221-184del
ENST00000641471.1:c.886-193_886-184del	ENSP00000493146.1:n.886-193_886-184del
ENST00000641691.1:c.*651-193_*651-184del	ENSP00000492910.1:n.*651-193_*651-184del
ENST00000641924.1:c.*228-193_*228-184del	ENSP00000493063.1:n.*228-193_*228-184del
ENST00000642050.2:c.799-193_799-184del MANE Select	ENSP00000493153.1:n.799-193_799-184del
ENST00000372775.2:n.196-193_196-184del
ENST00000433473.7:c.799-193_799-184del	ENSP00000394863.3:n.799-193_799-184del
ENST00000439754.5:c.412-193_412-184del	ENSP00000403207.1:n.412-193_412-184del
ENST00000449045.6:c.490-193_490-184del	ENSP00000392293.2:n.490-193_490-184del
ENST00000527311.6:c.574-193_574-184del	ENSP00000436695.2:n.574-193_574-184del
ENST00000529905.5:c.799-193_799-184del	ENSP00000432053.1:n.799-193_799-184del
ENST00000530076.5:c.142-193_142-184del	ENSP00000434007.1:n.142-193_142-184del
ENST00000530704.5:c.*422-193_*422-184del	ENSP00000431655.1:n.*422-193_*422-184del
NM_000310.3:c.799-193_799-184del , LRG_690t1:c.799-193_799-184del	NP_000301.1:n.799-193_799-184del
NM_001142604.1:c.490-193_490-184del	NP_001136076.1:n.490-193_490-184del
XM_005271008.1:c.727-193_727-184del	XP_005271065.1:n.727-193_727-184del
NM_001363695.1:c.727-193_727-184del	NP_001350624.1:n.727-193_727-184del
NM_000310.4:c.799-193_799-184del MANE Select	NP_000301.1:n.799-193_799-184del
NM_001142604.2:c.490-193_490-184del	NP_001136076.1:n.490-193_490-184del
NM_001363695.2:c.727-193_727-184del	NP_001350624.1:n.727-193_727-184del