Canonical Allele Identifier: CA2743277039

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40078880_40078882del , CM000663.2:g.40078880_40078882del	GRCh38
NC_000001.10:g.40544552_40544554del , CM000663.1:g.40544552_40544554del	GRCh37
NC_000001.9:g.40317139_40317141del	NCBI36
NG_009192.1:g.23589_23591del , LRG_690:g.23589_23591del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.625-224_625-222del	ENSP00000394863.4:n.625-224_625-222del
ENST00000439754.6:c.628-224_628-222del	ENSP00000403207.2:n.628-224_628-222del
ENST00000449045.7:c.319-224_319-222del	ENSP00000392293.2:n.319-224_319-222del
ENST00000527311.7:c.397-224_397-222del	ENSP00000436695.3:n.397-224_397-222del
ENST00000530076.6:c.-30-224_-30-222del	ENSP00000434007.1:n.-30-224_-30-222del
ENST00000530704.6:c.*251-224_*251-222del	ENSP00000431655.1:n.*251-224_*251-222del
ENST00000641083.1:c.606-224_606-222del
ENST00000641236.1:n.865-224_865-222del
ENST00000641319.1:c.628-224_628-222del	ENSP00000493128.1:n.628-224_628-222del
ENST00000641381.1:c.149-1969_149-1967del
ENST00000641471.1:c.715-224_715-222del	ENSP00000493146.1:n.715-224_715-222del
ENST00000641691.1:c.*480-224_*480-222del	ENSP00000492910.1:n.*480-224_*480-222del
ENST00000641924.1:c.*57-224_*57-222del	ENSP00000493063.1:n.*57-224_*57-222del
ENST00000642050.2:c.628-224_628-222del MANE Select	ENSP00000493153.1:n.628-224_628-222del
ENST00000372779.8:c.715-224_715-222del	ENSP00000361865.4:n.715-224_715-222del
ENST00000433473.7:c.628-224_628-222del	ENSP00000394863.3:n.628-224_628-222del
ENST00000439754.5:c.313-224_313-222del	ENSP00000403207.1:n.313-224_313-222del
ENST00000449045.6:c.319-224_319-222del	ENSP00000392293.2:n.319-224_319-222del
ENST00000527311.6:c.403-224_403-222del	ENSP00000436695.2:n.403-224_403-222del
ENST00000529905.5:c.628-224_628-222del	ENSP00000432053.1:n.628-224_628-222del
ENST00000530076.5:c.-30-224_-30-222del	ENSP00000434007.1:n.-30-224_-30-222del
ENST00000530704.5:c.*251-224_*251-222del	ENSP00000431655.1:n.*251-224_*251-222del
NM_000310.3:c.628-224_628-222del , LRG_690t1:c.628-224_628-222del	NP_000301.1:n.628-224_628-222del
NM_001142604.1:c.319-224_319-222del	NP_001136076.1:n.319-224_319-222del
XM_005271008.1:c.628-224_628-222del	XP_005271065.1:n.628-224_628-222del
NM_001363695.1:c.628-224_628-222del	NP_001350624.1:n.628-224_628-222del
NM_000310.4:c.628-224_628-222del MANE Select	NP_000301.1:n.628-224_628-222del
NM_001142604.2:c.319-224_319-222del	NP_001136076.1:n.319-224_319-222del
NM_001363695.2:c.628-224_628-222del	NP_001350624.1:n.628-224_628-222del