Canonical Allele Identifier: CA10645490

Gene: PLA2G6

Linked Data

• ClinVar Variation Id: 341627
• ClinVar RCV Id: RCV000278417
• dbSNP Id: rs45473603
• gnomAD v2: 22-38507627-G-A
• gnomAD v3: 22-38111620-G-A
• gnomAD v4: 22-38111620-G-A
• MyVariant Identifiers: chr22:g.38507627G>A (hg19) ; chr22:g.38111620G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38111620G>A , CM000684.2:g.38111620G>A	GRCh38
NC_000022.10:g.38507627G>A , CM000684.1:g.38507627G>A	GRCh37
NC_000022.9:g.36837573G>A	NCBI36
NG_007094.2:g.99071C>T
NG_033059.2:g.4050C>T
NG_007094.3:g.108159C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.*541C>T MANE Select	ENSP00000333142.3:n.*541C>T
ENST00000655142.1:c.*1820C>T	ENSP00000499715.1:n.*1820C>T
ENST00000663895.1:c.*541C>T	ENSP00000499712.1:n.*541C>T
ENST00000664587.1:c.*541C>T	ENSP00000499394.1:n.*541C>T
ENST00000668499.1:c.*2821C>T	ENSP00000499626.1:n.*2821C>T
ENST00000332509.7:c.*541C>T	ENSP00000333142.3:n.*541C>T
ENST00000335539.7:c.*541C>T	ENSP00000335149.3:n.*541C>T
ENST00000402064.5:c.*541C>T	ENSP00000386100.1:n.*541C>T
NM_001004426.1:c.*541C>T	NP_001004426.1:n.*541C>T
NM_001199562.1:c.*541C>T	NP_001186491.1:n.*541C>T
NM_003560.2:c.*541C>T	NP_003551.2:n.*541C>T
XM_005261764.1:c.*541C>T	XP_005261821.1:n.*541C>T
XM_005261765.1:c.*541C>T	XP_005261822.1:n.*541C>T
XM_005261766.1:c.*541C>T	XP_005261823.1:n.*541C>T
XM_006724332.2:c.*541C>T	XP_006724395.1:n.*541C>T
XM_011530422.1:c.*541C>T	XP_011528724.1:n.*541C>T
XM_011530423.1:c.*541C>T	XP_011528725.1:n.*541C>T
XM_011530424.1:c.*541C>T	XP_011528726.1:n.*541C>T
XM_011530425.1:c.*541C>T	XP_011528727.1:n.*541C>T
NM_001004426.2:c.*541C>T	NP_001004426.1:n.*541C>T
NM_001199562.2:c.*541C>T	NP_001186491.1:n.*541C>T
NM_001349864.1:c.*541C>T	NP_001336793.1:n.*541C>T
NM_001349865.1:c.*541C>T	NP_001336794.1:n.*541C>T
NM_001349866.1:c.*541C>T	NP_001336795.1:n.*541C>T
NM_001349867.1:c.*541C>T	NP_001336796.1:n.*541C>T
NM_001349868.1:c.*541C>T	NP_001336797.1:n.*541C>T
NM_001349869.1:c.*541C>T	NP_001336798.1:n.*541C>T
NM_003560.3:c.*541C>T	NP_003551.2:n.*541C>T
XM_005261764.3:c.*541C>T	XP_005261821.1:n.*541C>T
XM_005261765.2:c.*541C>T	XP_005261822.1:n.*541C>T
XM_006724332.4:c.*541C>T	XP_006724395.1:n.*541C>T
XM_017028983.1:c.*541C>T	XP_016884472.1:n.*541C>T
XM_024452280.1:c.*541C>T	XP_024308048.1:n.*541C>T
XM_024452281.1:c.*541C>T	XP_024308049.1:n.*541C>T
XM_024452282.1:c.*541C>T	XP_024308050.1:n.*541C>T
XM_024452283.1:c.*541C>T	XP_024308051.1:n.*541C>T
XM_024452284.1:c.*541C>T	XP_024308052.1:n.*541C>T
XM_024452285.1:c.*541C>T	XP_024308053.1:n.*541C>T
XR_001755325.2:n.3145C>T
XR_001755327.2:n.3140C>T
XR_001755328.2:n.3106C>T
NM_001199562.3:c.*541C>T	NP_001186491.1:n.*541C>T
NM_001349864.2:c.*541C>T	NP_001336793.1:n.*541C>T
NM_001349865.2:c.*541C>T	NP_001336794.1:n.*541C>T
NM_001349866.2:c.*541C>T	NP_001336795.1:n.*541C>T
NM_001349867.2:c.*541C>T	NP_001336796.1:n.*541C>T
NM_001349868.2:c.*541C>T	NP_001336797.1:n.*541C>T
NM_001349869.2:c.*541C>T	NP_001336798.1:n.*541C>T
NM_003560.4:c.*541C>T MANE Select	NP_003551.2:n.*541C>T
NM_001004426.3:c.*541C>T	NP_001004426.1:n.*541C>T