Canonical Allele Identifier: CA393786378
Gene: PLIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.90208126G>C (hg19) chr15:g.89664895G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89664895G>C , CM000677.2:g.89664895G>C GRCh38
NC_000015.9:g.90208126G>C , CM000677.1:g.90208126G>C GRCh37
NC_000015.8:g.88009130G>C NCBI36
NG_029172.1:g.19523C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300055.10:c.*688C>G MANE Select ENSP00000300055.5:n.*688C>G
ENST00000300055.9:c.*688C>G ENSP00000300055.5:n.*688C>G
ENST00000430628.2:c.*688C>G ENSP00000402167.2:n.*688C>G
ENST00000560330.1:c.170C>G ENSP00000453426.1:p.Thr57Ser
NM_001145311.1:c.*688C>G NP_001138783.1:n.*688C>G
NM_002666.4:c.*688C>G NP_002657.3:n.*688C>G
XM_005254934.3:c.*688C>G XP_005254991.1:n.*688C>G
XM_005254934.4:c.*688C>G XP_005254991.1:n.*688C>G
NM_002666.5:c.*688C>G MANE Select NP_002657.3:n.*688C>G
NM_001145311.2:c.*688C>G NP_001138783.1:n.*688C>G
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