Canonical Allele Identifier: CA2194719616
Gene: PLIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89664897G= , CM000677.2:g.89664897G= GRCh38
NC_000015.9:g.90208128G= , CM000677.1:g.90208128G= GRCh37
NC_000015.8:g.88009132G= NCBI36
NG_029172.1:g.19521C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300055.10:c.*686C= MANE Select ENSP00000300055.5:n.*686C=
ENST00000300055.9:c.*686C= ENSP00000300055.5:n.*686C=
ENST00000430628.2:c.*686C= ENSP00000402167.2:n.*686C=
ENST00000560330.1:c.168C= ENSP00000453426.1:p.Phe56=
NM_001145311.1:c.*686C= NP_001138783.1:n.*686C=
NM_002666.4:c.*686C= NP_002657.3:n.*686C=
XM_005254934.3:c.*686C= XP_005254991.1:n.*686C=
XM_005254934.4:c.*686C= XP_005254991.1:n.*686C=
NM_002666.5:c.*686C= MANE Select NP_002657.3:n.*686C=
NM_001145311.2:c.*686C= NP_001138783.1:n.*686C=