Canonical Allele Identifier: CA2739302791
Gene: PLIN1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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