Canonical Allele Identifier: CA2194719792
Community Standard Title: NM_002666.5(PLIN1):c.*504T=
Gene: PLIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89665079A= , CM000677.2:g.89665079A= GRCh38
NC_000015.9:g.90208310A= , CM000677.1:g.90208310A= GRCh37
NC_000015.8:g.88009314A= NCBI36
NG_029172.1:g.19339T=

Transcript Alleles

HGVS Amino-acid Change
NM_002666.5:c.*504T= MANE Select NP_002657.3:n.*504T=
ENST00000300055.10:c.*504T= MANE Select ENSP00000300055.5:n.*504T=
NM_001145311.1:c.*504T= NP_001138783.1:n.*504T=
NM_001145311.2:c.*504T= NP_001138783.1:n.*504T=
NM_002666.4:c.*504T= NP_002657.3:n.*504T=
ENST00000300055.9:c.*504T= ENSP00000300055.5:n.*504T=
ENST00000430628.2:c.*504T= ENSP00000402167.2:n.*504T=
ENST00000560330.1:c.124-138T= ENSP00000453426.1:n.124-138T=
XM_005254934.3:c.*504T= XP_005254991.1:n.*504T=
XM_005254934.4:c.*504T= XP_005254991.1:n.*504T=