Canonical Allele Identifier: CA411523746

Gene: PLA2G6

Linked Data

• MyVariant Identifiers: chr22:g.38509555G>C (hg19) ; chr22:g.38113548G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38113548G>C , CM000684.2:g.38113548G>C	GRCh38
NC_000022.10:g.38509555G>C , CM000684.1:g.38509555G>C	GRCh37
NC_000022.9:g.36839501G>C	NCBI36
NG_007094.2:g.97143C>G
NG_033059.2:g.2122C>G
NG_007094.3:g.106231C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332509.8:c.2141C>G MANE Select	ENSP00000333142.3:p.Pro714Arg
ENST00000436218.6:c.*1339C>G	ENSP00000401242.1:n.*1339C>G
ENST00000655142.1:c.*999C>G	ENSP00000499715.1:n.*999C>G
ENST00000660610.1:c.2141C>G	ENSP00000499555.1:p.Pro714Arg
ENST00000663895.1:c.2141C>G	ENSP00000499712.1:p.Pro714Arg
ENST00000664587.1:c.2003C>G	ENSP00000499394.1:p.Pro668Arg
ENST00000665987.1:c.*1880C>G	ENSP00000499423.1:n.*1880C>G
ENST00000667521.1:c.2141C>G	ENSP00000499665.1:p.Pro714Arg
ENST00000668499.1:c.*2000C>G	ENSP00000499626.1:n.*2000C>G
ENST00000668949.1:c.2183C>G	ENSP00000499711.1:p.Pro728Arg
ENST00000671093.1:n.2073C>G
ENST00000673413.1:c.*1810C>G	ENSP00000500600.1:n.*1810C>G
ENST00000332509.7:c.2141C>G	ENSP00000333142.3:p.Pro714Arg
ENST00000335539.7:c.1979C>G	ENSP00000335149.3:p.Pro660Arg
ENST00000402064.5:c.1979C>G	ENSP00000386100.1:p.Pro660Arg
ENST00000496409.1:n.849C>G
NM_001004426.1:c.1979C>G	NP_001004426.1:p.Pro660Arg
NM_001199562.1:c.1979C>G	NP_001186491.1:p.Pro660Arg
NM_003560.2:c.2141C>G	NP_003551.2:p.Pro714Arg
XM_005261764.1:c.2141C>G	XP_005261821.1:p.Pro714Arg
XM_005261765.1:c.2141C>G	XP_005261822.1:p.Pro714Arg
XM_005261766.1:c.2141C>G	XP_005261823.1:p.Pro714Arg
XM_006724332.2:c.2141C>G	XP_006724395.1:p.Pro714Arg
XM_011530422.1:c.2036C>G	XP_011528724.1:p.Pro679Arg
XM_011530423.1:c.1607C>G	XP_011528725.1:p.Pro536Arg
XM_011530424.1:c.1607C>G	XP_011528726.1:p.Pro536Arg
XM_011530425.1:c.1607C>G	XP_011528727.1:p.Pro536Arg
XR_244390.1:n.2417C>G
XR_430411.1:n.2301C>G
XR_937938.1:n.2503C>G
NM_001004426.2:c.1979C>G	NP_001004426.1:p.Pro660Arg
NM_001199562.2:c.1979C>G	NP_001186491.1:p.Pro660Arg
NM_001349864.1:c.2141C>G	NP_001336793.1:p.Pro714Arg
NM_001349865.1:c.1979C>G	NP_001336794.1:p.Pro660Arg
NM_001349866.1:c.1979C>G	NP_001336795.1:p.Pro660Arg
NM_001349867.1:c.1607C>G	NP_001336796.1:p.Pro536Arg
NM_001349868.1:c.1463C>G	NP_001336797.1:p.Pro488Arg
NM_001349869.1:c.1445C>G	NP_001336798.1:p.Pro482Arg
NM_003560.3:c.2141C>G	NP_003551.2:p.Pro714Arg
XM_005261764.3:c.2141C>G	XP_005261821.1:p.Pro714Arg
XM_005261765.2:c.2141C>G	XP_005261822.1:p.Pro714Arg
XM_006724332.4:c.2141C>G	XP_006724395.1:p.Pro714Arg
XM_017028983.1:c.1445C>G	XP_016884472.1:p.Pro482Arg
XM_024452280.1:c.1607C>G	XP_024308048.1:p.Pro536Arg
XM_024452281.1:c.1607C>G	XP_024308049.1:p.Pro536Arg
XM_024452282.1:c.1607C>G	XP_024308050.1:p.Pro536Arg
XM_024452283.1:c.1463C>G	XP_024308051.1:p.Pro488Arg
XM_024452284.1:c.1445C>G	XP_024308052.1:p.Pro482Arg
XM_024452285.1:c.1445C>G	XP_024308053.1:p.Pro482Arg
XR_001755325.2:n.2324C>G
XR_001755327.2:n.2319C>G
XR_001755328.2:n.2285C>G
XR_244390.3:n.2401C>G
XR_937938.3:n.2487C>G
NM_001199562.3:c.1979C>G	NP_001186491.1:p.Pro660Arg
NM_001349864.2:c.2141C>G	NP_001336793.1:p.Pro714Arg
NM_001349865.2:c.1979C>G	NP_001336794.1:p.Pro660Arg
NM_001349866.2:c.1979C>G	NP_001336795.1:p.Pro660Arg
NM_001349867.2:c.1607C>G	NP_001336796.1:p.Pro536Arg
NM_001349868.2:c.1463C>G	NP_001336797.1:p.Pro488Arg
NM_001349869.2:c.1445C>G	NP_001336798.1:p.Pro482Arg
NM_003560.4:c.2141C>G MANE Select	NP_003551.2:p.Pro714Arg
NM_001004426.3:c.1979C>G	NP_001004426.1:p.Pro660Arg