Canonical Allele Identifier: CA393786333

Gene: PLIN1

Linked Data

• MyVariant Identifiers: chr15:g.90208121T>A (hg19) ; chr15:g.89664890T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89664890T>A , CM000677.2:g.89664890T>A	GRCh38
NC_000015.9:g.90208121T>A , CM000677.1:g.90208121T>A	GRCh37
NC_000015.8:g.88009125T>A	NCBI36
NG_029172.1:g.19528A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300055.10:c.*693A>T MANE Select	ENSP00000300055.5:n.*693A>T
ENST00000300055.9:c.*693A>T	ENSP00000300055.5:n.*693A>T
ENST00000430628.2:c.*693A>T	ENSP00000402167.2:n.*693A>T
ENST00000560330.1:c.175A>T	ENSP00000453426.1:p.Ile59Leu
NM_001145311.1:c.*693A>T	NP_001138783.1:n.*693A>T
NM_002666.4:c.*693A>T	NP_002657.3:n.*693A>T
XM_005254934.3:c.*693A>T	XP_005254991.1:n.*693A>T
XM_005254934.4:c.*693A>T	XP_005254991.1:n.*693A>T
NM_002666.5:c.*693A>T MANE Select	NP_002657.3:n.*693A>T
NM_001145311.2:c.*693A>T	NP_001138783.1:n.*693A>T