Canonical Allele Identifier: CA2194719612
Gene: PLIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89664895G= , CM000677.2:g.89664895G= GRCh38
NC_000015.9:g.90208126G= , CM000677.1:g.90208126G= GRCh37
NC_000015.8:g.88009130G= NCBI36
NG_029172.1:g.19523C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300055.10:c.*688C= MANE Select ENSP00000300055.5:n.*688C=
ENST00000300055.9:c.*688C= ENSP00000300055.5:n.*688C=
ENST00000430628.2:c.*688C= ENSP00000402167.2:n.*688C=
ENST00000560330.1:c.170C= ENSP00000453426.1:p.Thr57=
NM_001145311.1:c.*688C= NP_001138783.1:n.*688C=
NM_002666.4:c.*688C= NP_002657.3:n.*688C=
XM_005254934.3:c.*688C= XP_005254991.1:n.*688C=
XM_005254934.4:c.*688C= XP_005254991.1:n.*688C=
NM_002666.5:c.*688C= MANE Select NP_002657.3:n.*688C=
NM_001145311.2:c.*688C= NP_001138783.1:n.*688C=