Canonical Allele Identifier: CA9140641
Gene: PNPLA6 HGNC NCBI

Linked Data

ClinVar Variation Id: 510462
dbSNP Id: rs371325894
gnomAD v2: 19-7626083-C-T
gnomAD v3: 19-7561197-C-T
gnomAD v4: 19-7561197-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7561197C>T , CM000681.2:g.7561197C>T GRCh38
NC_000019.9:g.7626083C>T , CM000681.1:g.7626083C>T GRCh37
NC_000019.8:g.7532083C>T NCBI36
NG_013374.1:g.32046C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000600737.6:c.3914-11C>T MANE Select ENSP00000473211.1:n.3914-11C>T
ENST00000221249.10:c.3800-11C>T ENSP00000221249.5:n.3800-11C>T
ENST00000414982.7:c.3944-11C>T ENSP00000407509.2:n.3944-11C>T
ENST00000450331.7:c.3800-11C>T ENSP00000394348.2:n.3800-11C>T
ENST00000545201.6:c.3719-11C>T ENSP00000443323.1:n.3719-11C>T
ENST00000597202.1:n.272-11C>T
ENST00000599947.1:c.283-11C>T
ENST00000600737.5:c.3914-11C>T ENSP00000473211.1:n.3914-11C>T
NM_001166111.1:c.3944-11C>T NP_001159583.1:n.3944-11C>T
NM_001166112.1:c.3719-11C>T NP_001159584.1:n.3719-11C>T
NM_001166113.1:c.3800-11C>T NP_001159585.1:n.3800-11C>T
NM_001166114.1:c.3914-11C>T NP_001159586.1:n.3914-11C>T
NM_006702.4:c.3800-11C>T NP_006693.3:n.3800-11C>T
NM_001166111.2:c.3944-11C>T NP_001159583.1:n.3944-11C>T
NM_001166114.2:c.3914-11C>T MANE Select NP_001159586.1:n.3914-11C>T
NM_006702.5:c.3800-11C>T NP_006693.3:n.3800-11C>T
NM_001166112.2:c.3719-11C>T NP_001159584.1:n.3719-11C>T