Canonical Allele Identifier: CA2743276140

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074350_40074351insACA , CM000663.2:g.40074350_40074351insACA	GRCh38
NC_000001.10:g.40540022_40540023insACA , CM000663.1:g.40540022_40540023insACA	GRCh37
NC_000001.9:g.40312609_40312610insACA	NCBI36
NG_009192.1:g.28120_28121insTGT , LRG_690:g.28120_28121insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.796-168_796-167insTGT	ENSP00000394863.4:n.796-168_796-167insTGT
ENST00000439754.6:c.727-168_727-167insTGT	ENSP00000403207.2:n.727-168_727-167insTGT
ENST00000449045.7:c.490-168_490-167insTGT	ENSP00000392293.2:n.490-168_490-167insTGT
ENST00000527311.7:c.568-168_568-167insTGT	ENSP00000436695.3:n.568-168_568-167insTGT
ENST00000530076.6:c.142-168_142-167insTGT	ENSP00000434007.1:n.142-168_142-167insTGT
ENST00000530704.6:c.*422-168_*422-167insTGT	ENSP00000431655.1:n.*422-168_*422-167insTGT
ENST00000641083.1:c.889-168_889-167insTGT
ENST00000641236.1:n.1036-168_1036-167insTGT
ENST00000641319.1:c.*9-168_*9-167insTGT	ENSP00000493128.1:n.*9-168_*9-167insTGT
ENST00000641381.1:c.221-168_221-167insTGT
ENST00000641471.1:c.886-168_886-167insTGT	ENSP00000493146.1:n.886-168_886-167insTGT
ENST00000641691.1:c.*651-168_*651-167insTGT	ENSP00000492910.1:n.*651-168_*651-167insTGT
ENST00000641924.1:c.*228-168_*228-167insTGT	ENSP00000493063.1:n.*228-168_*228-167insTGT
ENST00000642050.2:c.799-168_799-167insTGT MANE Select	ENSP00000493153.1:n.799-168_799-167insTGT
ENST00000372775.2:n.196-168_196-167insTGT
ENST00000433473.7:c.799-168_799-167insTGT	ENSP00000394863.3:n.799-168_799-167insTGT
ENST00000439754.5:c.412-168_412-167insTGT	ENSP00000403207.1:n.412-168_412-167insTGT
ENST00000449045.6:c.490-168_490-167insTGT	ENSP00000392293.2:n.490-168_490-167insTGT
ENST00000527311.6:c.574-168_574-167insTGT	ENSP00000436695.2:n.574-168_574-167insTGT
ENST00000529905.5:c.799-168_799-167insTGT	ENSP00000432053.1:n.799-168_799-167insTGT
ENST00000530076.5:c.142-168_142-167insTGT	ENSP00000434007.1:n.142-168_142-167insTGT
ENST00000530704.5:c.*422-168_*422-167insTGT	ENSP00000431655.1:n.*422-168_*422-167insTGT
NM_000310.3:c.799-168_799-167insTGT , LRG_690t1:c.799-168_799-167insTGT	NP_000301.1:n.799-168_799-167insTGT
NM_001142604.1:c.490-168_490-167insTGT	NP_001136076.1:n.490-168_490-167insTGT
XM_005271008.1:c.727-168_727-167insTGT	XP_005271065.1:n.727-168_727-167insTGT
NM_001363695.1:c.727-168_727-167insTGT	NP_001350624.1:n.727-168_727-167insTGT
NM_000310.4:c.799-168_799-167insTGT MANE Select	NP_000301.1:n.799-168_799-167insTGT
NM_001142604.2:c.490-168_490-167insTGT	NP_001136076.1:n.490-168_490-167insTGT
NM_001363695.2:c.727-168_727-167insTGT	NP_001350624.1:n.727-168_727-167insTGT