Canonical Allele Identifier: CA393786420

Gene: PLIN1

Linked Data

• gnomAD v4: 15-89664902-C-A
• MyVariant Identifiers: chr15:g.90208133C>A (hg19) ; chr15:g.89664902C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89664902C>A , CM000677.2:g.89664902C>A	GRCh38
NC_000015.9:g.90208133C>A , CM000677.1:g.90208133C>A	GRCh37
NC_000015.8:g.88009137C>A	NCBI36
NG_029172.1:g.19516G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300055.10:c.*681G>T MANE Select	ENSP00000300055.5:n.*681G>T
ENST00000300055.9:c.*681G>T	ENSP00000300055.5:n.*681G>T
ENST00000430628.2:c.*681G>T	ENSP00000402167.2:n.*681G>T
ENST00000560330.1:c.163G>T	ENSP00000453426.1:p.Ala55Ser
NM_001145311.1:c.*681G>T	NP_001138783.1:n.*681G>T
NM_002666.4:c.*681G>T	NP_002657.3:n.*681G>T
XM_005254934.3:c.*681G>T	XP_005254991.1:n.*681G>T
XM_005254934.4:c.*681G>T	XP_005254991.1:n.*681G>T
NM_002666.5:c.*681G>T MANE Select	NP_002657.3:n.*681G>T
NM_001145311.2:c.*681G>T	NP_001138783.1:n.*681G>T