Canonical Allele Identifier: CA2194719713
Gene: PLIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89665000A= , CM000677.2:g.89665000A= GRCh38
NC_000015.9:g.90208231A= , CM000677.1:g.90208231A= GRCh37
NC_000015.8:g.88009235A= NCBI36
NG_029172.1:g.19418T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300055.10:c.*583T= MANE Select ENSP00000300055.5:n.*583T=
ENST00000300055.9:c.*583T= ENSP00000300055.5:n.*583T=
ENST00000430628.2:c.*583T= ENSP00000402167.2:n.*583T=
ENST00000560330.1:c.124-59T= ENSP00000453426.1:n.124-59T=
NM_001145311.1:c.*583T= NP_001138783.1:n.*583T=
NM_002666.4:c.*583T= NP_002657.3:n.*583T=
XM_005254934.3:c.*583T= XP_005254991.1:n.*583T=
XM_005254934.4:c.*583T= XP_005254991.1:n.*583T=
NM_002666.5:c.*583T= MANE Select NP_002657.3:n.*583T=
NM_001145311.2:c.*583T= NP_001138783.1:n.*583T=