Canonical Allele Identifier: CA2194719618
Gene: PLIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89664900G= , CM000677.2:g.89664900G= GRCh38
NC_000015.9:g.90208131G= , CM000677.1:g.90208131G= GRCh37
NC_000015.8:g.88009135G= NCBI36
NG_029172.1:g.19518C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300055.10:c.*683C= MANE Select ENSP00000300055.5:n.*683C=
ENST00000300055.9:c.*683C= ENSP00000300055.5:n.*683C=
ENST00000430628.2:c.*683C= ENSP00000402167.2:n.*683C=
ENST00000560330.1:c.165C= ENSP00000453426.1:p.Ala55=
NM_001145311.1:c.*683C= NP_001138783.1:n.*683C=
NM_002666.4:c.*683C= NP_002657.3:n.*683C=
XM_005254934.3:c.*683C= XP_005254991.1:n.*683C=
XM_005254934.4:c.*683C= XP_005254991.1:n.*683C=
NM_002666.5:c.*683C= MANE Select NP_002657.3:n.*683C=
NM_001145311.2:c.*683C= NP_001138783.1:n.*683C=