Canonical Allele Identifier: CA2574329791

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092007_40092011del , CM000663.2:g.40092007_40092011del	GRCh38
NC_000001.10:g.40557679_40557683del , CM000663.1:g.40557679_40557683del	GRCh37
NC_000001.9:g.40330266_40330270del	NCBI36
NG_009192.1:g.10462_10466del , LRG_690:g.10462_10466del

Transcript Alleles

HGVS	Amino-acid change
ENST00000372779.9:c.*198+36_*198+40del	ENSP00000361865.5:n.*198+36_*198+40del
ENST00000433473.8:c.359+36_359+40del	ENSP00000394863.4:n.359+36_359+40del
ENST00000439754.6:c.362+36_362+40del	ENSP00000403207.2:n.362+36_362+40del
ENST00000449045.7:c.125-2497_125-2493del	ENSP00000392293.2:n.125-2497_125-2493del
ENST00000526547.2:c.642+36_642+40del
ENST00000527311.7:c.234+389_234+393del	ENSP00000436695.3:n.234+389_234+393del
ENST00000530704.6:c.362+36_362+40del	ENSP00000431655.1:n.362+36_362+40del
ENST00000641083.1:c.340+36_340+40del
ENST00000641236.1:n.599+36_599+40del
ENST00000641319.1:c.362+36_362+40del	ENSP00000493128.1:n.362+36_362+40del
ENST00000641471.1:c.449+36_449+40del	ENSP00000493146.1:n.449+36_449+40del
ENST00000641548.1:c.*214+36_*214+40del	ENSP00000492984.1:n.*214+36_*214+40del
ENST00000641691.1:c.*214+36_*214+40del	ENSP00000492910.1:n.*214+36_*214+40del
ENST00000641924.1:c.124+5106_124+5110del	ENSP00000493063.1:n.124+5106_124+5110del
ENST00000642050.2:c.362+36_362+40del MANE Select	ENSP00000493153.1:n.362+36_362+40del
ENST00000372779.8:c.449+36_449+40del	ENSP00000361865.4:n.449+36_449+40del
ENST00000433473.7:c.362+36_362+40del	ENSP00000394863.3:n.362+36_362+40del
ENST00000439754.5:c.47+36_47+40del	ENSP00000403207.1:n.47+36_47+40del
ENST00000449045.6:c.125-2497_125-2493del	ENSP00000392293.2:n.125-2497_125-2493del
ENST00000526547.1:c.212+36_212+40del	ENSP00000436481.1:n.212+36_212+40del
ENST00000527311.6:c.137+36_137+40del	ENSP00000436695.2:n.137+36_137+40del
ENST00000529905.5:c.362+36_362+40del	ENSP00000432053.1:n.362+36_362+40del
ENST00000530704.5:c.362+36_362+40del	ENSP00000431655.1:n.362+36_362+40del
NM_000310.3:c.362+36_362+40del , LRG_690t1:c.362+36_362+40del	NP_000301.1:n.362+36_362+40del
NM_001142604.1:c.125-2497_125-2493del	NP_001136076.1:n.125-2497_125-2493del
XM_005271008.1:c.362+36_362+40del	XP_005271065.1:n.362+36_362+40del
NM_001363695.1:c.362+36_362+40del	NP_001350624.1:n.362+36_362+40del
NM_000310.4:c.362+36_362+40del MANE Select	NP_000301.1:n.362+36_362+40del
NM_001142604.2:c.125-2497_125-2493del	NP_001136076.1:n.125-2497_125-2493del
NM_001363695.2:c.362+36_362+40del	NP_001350624.1:n.362+36_362+40del