Canonical Allele Identifier: CA411523416

Gene: PLA2G6

Linked Data

• gnomAD v4: 22-38112570-T-A
• MyVariant Identifiers: chr22:g.38508577T>A (hg19) ; chr22:g.38112570T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38112570T>A , CM000684.2:g.38112570T>A	GRCh38
NC_000022.10:g.38508577T>A , CM000684.1:g.38508577T>A	GRCh37
NC_000022.9:g.36838523T>A	NCBI36
NG_007094.2:g.98121A>T
NG_033059.2:g.3100A>T
NG_007094.3:g.107209A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332509.8:c.2210A>T MANE Select	ENSP00000333142.3:p.Asp737Val
ENST00000436218.6:c.*1408A>T	ENSP00000401242.1:n.*1408A>T
ENST00000655142.1:c.*1068A>T	ENSP00000499715.1:n.*1068A>T
ENST00000660610.1:c.2210A>T	ENSP00000499555.1:p.Asp737Val
ENST00000663895.1:c.2210A>T	ENSP00000499712.1:p.Asp737Val
ENST00000664587.1:c.2072A>T	ENSP00000499394.1:p.Asp691Val
ENST00000665987.1:c.*1949A>T	ENSP00000499423.1:n.*1949A>T
ENST00000667521.1:c.2210A>T	ENSP00000499665.1:p.Asp737Val
ENST00000668499.1:c.*2069A>T	ENSP00000499626.1:n.*2069A>T
ENST00000668949.1:c.2252A>T	ENSP00000499711.1:p.Asp751Val
ENST00000671093.1:n.2142A>T
ENST00000673413.1:c.*1879A>T	ENSP00000500600.1:n.*1879A>T
ENST00000332509.7:c.2210A>T	ENSP00000333142.3:p.Asp737Val
ENST00000335539.7:c.2048A>T	ENSP00000335149.3:p.Asp683Val
ENST00000402064.5:c.2048A>T	ENSP00000386100.1:p.Asp683Val
ENST00000463287.1:n.286A>T
NM_001004426.1:c.2048A>T	NP_001004426.1:p.Asp683Val
NM_001199562.1:c.2048A>T	NP_001186491.1:p.Asp683Val
NM_003560.2:c.2210A>T	NP_003551.2:p.Asp737Val
XM_005261764.1:c.2210A>T	XP_005261821.1:p.Asp737Val
XM_005261765.1:c.2210A>T	XP_005261822.1:p.Asp737Val
XM_005261766.1:c.2210A>T	XP_005261823.1:p.Asp737Val
XM_006724332.2:c.2210A>T	XP_006724395.1:p.Asp737Val
XM_011530422.1:c.2105A>T	XP_011528724.1:p.Asp702Val
XM_011530423.1:c.1676A>T	XP_011528725.1:p.Asp559Val
XM_011530424.1:c.1676A>T	XP_011528726.1:p.Asp559Val
XM_011530425.1:c.1676A>T	XP_011528727.1:p.Asp559Val
NM_001004426.2:c.2048A>T	NP_001004426.1:p.Asp683Val
NM_001199562.2:c.2048A>T	NP_001186491.1:p.Asp683Val
NM_001349864.1:c.2210A>T	NP_001336793.1:p.Asp737Val
NM_001349865.1:c.2048A>T	NP_001336794.1:p.Asp683Val
NM_001349866.1:c.2048A>T	NP_001336795.1:p.Asp683Val
NM_001349867.1:c.1676A>T	NP_001336796.1:p.Asp559Val
NM_001349868.1:c.1532A>T	NP_001336797.1:p.Asp511Val
NM_001349869.1:c.1514A>T	NP_001336798.1:p.Asp505Val
NM_003560.3:c.2210A>T	NP_003551.2:p.Asp737Val
XM_005261764.3:c.2210A>T	XP_005261821.1:p.Asp737Val
XM_005261765.2:c.2210A>T	XP_005261822.1:p.Asp737Val
XM_006724332.4:c.2210A>T	XP_006724395.1:p.Asp737Val
XM_017028983.1:c.1514A>T	XP_016884472.1:p.Asp505Val
XM_024452280.1:c.1676A>T	XP_024308048.1:p.Asp559Val
XM_024452281.1:c.1676A>T	XP_024308049.1:p.Asp559Val
XM_024452282.1:c.1676A>T	XP_024308050.1:p.Asp559Val
XM_024452283.1:c.1532A>T	XP_024308051.1:p.Asp511Val
XM_024452284.1:c.1514A>T	XP_024308052.1:p.Asp505Val
XM_024452285.1:c.1514A>T	XP_024308053.1:p.Asp505Val
XR_001755325.2:n.2393A>T
XR_001755327.2:n.2388A>T
XR_001755328.2:n.2354A>T
NM_001199562.3:c.2048A>T	NP_001186491.1:p.Asp683Val
NM_001349864.2:c.2210A>T	NP_001336793.1:p.Asp737Val
NM_001349865.2:c.2048A>T	NP_001336794.1:p.Asp683Val
NM_001349866.2:c.2048A>T	NP_001336795.1:p.Asp683Val
NM_001349867.2:c.1676A>T	NP_001336796.1:p.Asp559Val
NM_001349868.2:c.1532A>T	NP_001336797.1:p.Asp511Val
NM_001349869.2:c.1514A>T	NP_001336798.1:p.Asp505Val
NM_003560.4:c.2210A>T MANE Select	NP_003551.2:p.Asp737Val
NM_001004426.3:c.2048A>T	NP_001004426.1:p.Asp683Val