Canonical Allele Identifier: CA1164251249
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40091269_40091270delinsTA , CM000663.2:g.40091269_40091270delinsTA GRCh38
NC_000001.10:g.40556941_40556942delinsTA , CM000663.1:g.40556941_40556942delinsTA GRCh37
NC_000001.9:g.40329528_40329529delinsTA NCBI36
NG_009192.1:g.11201_11202delinsTA , LRG_690:g.11201_11202delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.*269+59_*269+60delinsTA ENSP00000361865.5:n.*269+59_*269+60delins...
ENST00000433473.8:c.430+59_430+60delinsTA ENSP00000394863.4:n.430+59_430+60delinsTA...
ENST00000439754.6:c.433+59_433+60delinsTA ENSP00000403207.2:n.433+59_433+60delinsTA...
ENST00000449045.7:c.125-1758_125-1757delinsTA ENSP00000392293.2:n.125-1758_125-1757deli...
ENST00000526547.2:c.713+59_713+60delinsTA
ENST00000527311.7:c.305+59_305+60delinsTA ENSP00000436695.3:n.305+59_305+60delinsTA...
ENST00000530704.6:c.433+59_433+60delinsTA ENSP00000431655.1:n.433+59_433+60delinsTA...
ENST00000641083.1:c.411+59_411+60delinsTA
ENST00000641236.1:n.670+59_670+60delinsTA
ENST00000641319.1:c.433+59_433+60delinsTA ENSP00000493128.1:n.433+59_433+60delinsTA...
ENST00000641381.1:c.45+59_45+60delinsTA
ENST00000641471.1:c.520+59_520+60delinsTA ENSP00000493146.1:n.520+59_520+60delinsTA...
ENST00000641548.1:c.*285+59_*285+60delinsTA ENSP00000492984.1:n.*285+59_*285+60delins...
ENST00000641691.1:c.*285+59_*285+60delinsTA ENSP00000492910.1:n.*285+59_*285+60delins...
ENST00000641924.1:c.124+5845_124+5846delinsTA ENSP00000493063.1:n.124+5845_124+5846deli...
ENST00000642050.2:c.433+59_433+60delinsTA MANE Select ENSP00000493153.1:n.433+59_433+60delinsTA...
ENST00000372779.8:c.520+59_520+60delinsTA ENSP00000361865.4:n.520+59_520+60delinsTA...
ENST00000433473.7:c.433+59_433+60delinsTA ENSP00000394863.3:n.433+59_433+60delinsTA...
ENST00000439754.5:c.118+59_118+60delinsTA ENSP00000403207.1:n.118+59_118+60delinsTA...
ENST00000449045.6:c.125-1758_125-1757delinsTA ENSP00000392293.2:n.125-1758_125-1757deli...
ENST00000526547.1:c.283+59_283+60delinsTA ENSP00000436481.1:n.283+59_283+60delinsTA...
ENST00000527311.6:c.208+59_208+60delinsTA ENSP00000436695.2:n.208+59_208+60delinsTA...
ENST00000529905.5:c.433+59_433+60delinsTA ENSP00000432053.1:n.433+59_433+60delinsTA...
ENST00000530704.5:c.433+59_433+60delinsTA ENSP00000431655.1:n.433+59_433+60delinsTA...
NM_000310.3:c.433+59_433+60delinsTA , LRG_690t1:c.433+59_433+60delinsTA NP_000301.1:n.433+59_433+60delinsTA
NM_001142604.1:c.125-1758_125-1757delinsTA NP_001136076.1:n.125-1758_125-1757delinsT...
XM_005271008.1:c.433+59_433+60delinsTA XP_005271065.1:n.433+59_433+60delinsTA
NM_001363695.1:c.433+59_433+60delinsTA NP_001350624.1:n.433+59_433+60delinsTA
NM_000310.4:c.433+59_433+60delinsTA MANE Select NP_000301.1:n.433+59_433+60delinsTA
NM_001142604.2:c.125-1758_125-1757delinsTA NP_001136076.1:n.125-1758_125-1757delinsT...
NM_001363695.2:c.433+59_433+60delinsTA NP_001350624.1:n.433+59_433+60delinsTA