Canonical Allele Identifier: CA2194719710
Gene: PLIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89664996A= , CM000677.2:g.89664996A= GRCh38
NC_000015.9:g.90208227A= , CM000677.1:g.90208227A= GRCh37
NC_000015.8:g.88009231A= NCBI36
NG_029172.1:g.19422T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300055.10:c.*587T= MANE Select ENSP00000300055.5:n.*587T=
ENST00000300055.9:c.*587T= ENSP00000300055.5:n.*587T=
ENST00000430628.2:c.*587T= ENSP00000402167.2:n.*587T=
ENST00000560330.1:c.124-55T= ENSP00000453426.1:n.124-55T=
NM_001145311.1:c.*587T= NP_001138783.1:n.*587T=
NM_002666.4:c.*587T= NP_002657.3:n.*587T=
XM_005254934.3:c.*587T= XP_005254991.1:n.*587T=
XM_005254934.4:c.*587T= XP_005254991.1:n.*587T=
NM_002666.5:c.*587T= MANE Select NP_002657.3:n.*587T=
NM_001145311.2:c.*587T= NP_001138783.1:n.*587T=