Canonical Allele Identifier: CA9142845

Gene: PET100

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7630795G>A , CM000681.2:g.7630795G>A	GRCh38
NC_000019.9:g.7695681G>A , CM000681.1:g.7695681G>A	GRCh37
NC_000019.8:g.7601681G>A	NCBI36
NG_034117.1:g.6011G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001171155.2:c.115-28G>A MANE Select	NP_001164626.1:n.115-28G>A
ENST00000594797.6:c.115-28G>A MANE Select	ENSP00000470539.1:n.115-28G>A
NM_001171155.1:c.115-28G>A	NP_001164626.1:n.115-28G>A
NR_033242.1:n.164-28G>A
NR_033242.2:n.156-28G>A
ENST00000456958.7:c.28-28G>A	ENSP00000392303.3:n.28-28G>A
ENST00000594797.5:c.115-28G>A	ENSP00000470539.1:n.115-28G>A
ENST00000595866.1:c.113-28G>A
ENST00000595866.2:c.115-28G>A	ENSP00000469553.2:n.115-28G>A
ENST00000598540.6:c.110-28G>A
ENST00000598664.5:c.28-28G>A	ENSP00000472796.1:n.28-28G>A
ENST00000599243.5:c.115-28G>A	ENSP00000470078.1:n.115-28G>A
ENST00000600836.1:n.271G>A
ENST00000601406.5:c.115-28G>A	ENSP00000470935.1:n.115-28G>A
ENST00000601829.1:n.260G>A
ENST00000623154.1:n.987G>A
ENST00000698367.1:n.62-28G>A
ENST00000698368.1:c.114+136G>A	ENSP00000513686.1:n.114+136G>A
ENST00000698396.1:c.64-28G>A	ENSP00000513691.1:n.64-28G>A
ENST00000698397.1:c.115-28G>A	ENSP00000513692.1:n.115-28G>A
ENST00000698398.1:c.153G>A	ENSP00000513693.1:n.153G>A