Canonical Allele Identifier: CA393786696

Gene: PLIN1

Linked Data

• MyVariant Identifiers: chr15:g.90208159C>A (hg19) ; chr15:g.89664928C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89664928C>A , CM000677.2:g.89664928C>A	GRCh38
NC_000015.9:g.90208159C>A , CM000677.1:g.90208159C>A	GRCh37
NC_000015.8:g.88009163C>A	NCBI36
NG_029172.1:g.19490G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300055.10:c.*655G>T MANE Select	ENSP00000300055.5:n.*655G>T
ENST00000300055.9:c.*655G>T	ENSP00000300055.5:n.*655G>T
ENST00000430628.2:c.*655G>T	ENSP00000402167.2:n.*655G>T
ENST00000560330.1:c.137G>T	ENSP00000453426.1:p.Ser46Ile
NM_001145311.1:c.*655G>T	NP_001138783.1:n.*655G>T
NM_002666.4:c.*655G>T	NP_002657.3:n.*655G>T
XM_005254934.3:c.*655G>T	XP_005254991.1:n.*655G>T
XM_005254934.4:c.*655G>T	XP_005254991.1:n.*655G>T
NM_002666.5:c.*655G>T MANE Select	NP_002657.3:n.*655G>T
NM_001145311.2:c.*655G>T	NP_001138783.1:n.*655G>T