Canonical Allele Identifier: CA393786392
Gene: PLIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.90208129A>T (hg19) chr15:g.89664898A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89664898A>T , CM000677.2:g.89664898A>T GRCh38
NC_000015.9:g.90208129A>T , CM000677.1:g.90208129A>T GRCh37
NC_000015.8:g.88009133A>T NCBI36
NG_029172.1:g.19520T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000300055.10:c.*685T>A MANE Select ENSP00000300055.5:n.*685T>A
ENST00000300055.9:c.*685T>A ENSP00000300055.5:n.*685T>A
ENST00000430628.2:c.*685T>A ENSP00000402167.2:n.*685T>A
ENST00000560330.1:c.167T>A ENSP00000453426.1:p.Phe56Tyr
NM_001145311.1:c.*685T>A NP_001138783.1:n.*685T>A
NM_002666.4:c.*685T>A NP_002657.3:n.*685T>A
XM_005254934.3:c.*685T>A XP_005254991.1:n.*685T>A
XM_005254934.4:c.*685T>A XP_005254991.1:n.*685T>A
NM_002666.5:c.*685T>A MANE Select NP_002657.3:n.*685T>A
NM_001145311.2:c.*685T>A NP_001138783.1:n.*685T>A
Search 100 bp 5'
Search 100 bp 3'