Canonical Allele Identifier: CA2194723406
Gene: PLIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89668592C= , CM000677.2:g.89668592C= GRCh38
NC_000015.9:g.90211823C= , CM000677.1:g.90211823C= GRCh37
NC_000015.8:g.88012827C= NCBI36
NG_029172.1:g.15826G=

Transcript Alleles

HGVS Amino-acid Change
NM_002666.5:c.772-799G= MANE Select NP_002657.3:n.772-799G=
ENST00000300055.10:c.772-799G= MANE Select ENSP00000300055.5:n.772-799G=
NM_001145311.1:c.772-799G= NP_001138783.1:n.772-799G=
NM_001145311.2:c.772-799G= NP_001138783.1:n.772-799G=
NM_002666.4:c.772-799G= NP_002657.3:n.772-799G=
ENST00000300055.9:c.772-799G= ENSP00000300055.5:n.772-799G=
ENST00000430628.2:c.772-799G= ENSP00000402167.2:n.772-799G=
XM_005254934.3:c.772-799G= XP_005254991.1:n.772-799G=
XM_005254934.4:c.772-799G= XP_005254991.1:n.772-799G=