Canonical Allele Identifier: CA403446827

Gene: PLIN4

Linked Data

• ClinVar Variation Id: 3215280
• ClinVar RCV Id: RCV004506610
• MyVariant Identifiers: chr19:g.4504737A>C (hg19) ; chr19:g.4504725A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4504725A>C , CM000681.2:g.4504725A>C	GRCh38
NC_000019.9:g.4504737A>C , CM000681.1:g.4504737A>C	GRCh37
NC_000019.8:g.4455737A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301286.5:c.3850T>G MANE Select	ENSP00000301286.4:p.Tyr1284Asp
ENST00000301286.4:c.3808T>G	ENSP00000301286.3:p.Tyr1270Asp
ENST00000633942.1:c.3853T>G	ENSP00000488481.1:p.Tyr1285Asp
NM_001080400.1:c.3808T>G	NP_001073869.1:p.Tyr1270Asp
XM_006722866.1:c.3853T>G	XP_006722929.1:p.Tyr1285Asp
XM_006722868.2:c.3850T>G	XP_006722931.1:p.Tyr1284Asp
XM_011528233.1:c.4033T>G	XP_011526535.1:p.Tyr1345Asp
XM_011528234.1:c.4033T>G	XP_011526536.1:p.Tyr1345Asp
XM_011528235.1:c.4033T>G	XP_011526537.1:p.Tyr1345Asp
XM_011528236.1:c.3736T>G	XP_011526538.1:p.Tyr1246Asp
XM_011528237.1:c.3637T>G	XP_011526539.1:p.Tyr1213Asp
XM_006722866.2:c.3853T>G	XP_006722929.1:p.Tyr1285Asp
XM_006722868.4:c.3850T>G	XP_006722931.1:p.Tyr1284Asp
XM_011528233.2:c.4033T>G	XP_011526535.1:p.Tyr1345Asp
XM_017027192.1:c.4036T>G	XP_016882681.1:p.Tyr1346Asp
XM_017027193.1:c.4036T>G	XP_016882682.1:p.Tyr1346Asp
XM_017027194.1:c.4036T>G	XP_016882683.1:p.Tyr1346Asp
NM_001367868.1:c.3850T>G	NP_001354797.1:p.Tyr1284Asp
NM_001367868.2:c.3850T>G MANE Select	NP_001354797.1:p.Tyr1284Asp
NM_001393888.1:c.3853T>G	NP_001380817.1:p.Tyr1285Asp
NM_001393889.1:c.3853T>G	NP_001380818.1:p.Tyr1285Asp
NM_001393890.1:c.3850T>G	NP_001380819.1:p.Tyr1284Asp
NM_001393891.1:c.3850T>G	NP_001380820.1:p.Tyr1284Asp