Canonical Allele Identifier: CA2339716648

Gene: PLA2G4C

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48060277A>C , CM000681.2:g.48060277A>C	GRCh38
NC_000019.9:g.48563534A>C , CM000681.1:g.48563534A>C	GRCh37
NC_000019.8:g.53255346A>C	NCBI36
NG_016021.1:g.55576T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599921.6:c.1257+1721T>G MANE Select	ENSP00000469473.1:n.1257+1721T>G
ENST00000354276.7:c.1257+1721T>G	ENSP00000346228.2:n.1257+1721T>G
ENST00000596353.1:n.296+1721T>G
ENST00000596510.5:n.967+1721T>G
ENST00000599111.5:c.1287+1721T>G	ENSP00000472546.1:n.1287+1721T>G
ENST00000599300.5:c.513+1721T>G	ENSP00000470418.1:n.513+1721T>G
ENST00000599921.5:c.1257+1721T>G	ENSP00000469473.1:n.1257+1721T>G
NM_001159322.1:c.1287+1721T>G	NP_001152794.1:n.1287+1721T>G
NM_001159323.1:c.1257+1721T>G	NP_001152795.1:n.1257+1721T>G
NM_003706.2:c.1257+1721T>G	NP_003697.2:n.1257+1721T>G
XM_011527431.1:c.1203+1721T>G	XP_011525733.1:n.1203+1721T>G
XM_011527434.1:c.720+1721T>G	XP_011525736.1:n.720+1721T>G
XM_011527431.3:c.1203+1721T>G	XP_011525733.1:n.1203+1721T>G
XM_017027411.2:c.1203+1721T>G	XP_016882900.1:n.1203+1721T>G
XM_017027412.2:c.720+1721T>G	XP_016882901.1:n.720+1721T>G
XM_017027413.2:c.720+1721T>G	XP_016882902.1:n.720+1721T>G
NM_003706.3:c.1257+1721T>G MANE Select	NP_003697.2:n.1257+1721T>G
NM_001159322.2:c.1287+1721T>G	NP_001152794.1:n.1287+1721T>G
NM_001159323.2:c.1257+1721T>G	NP_001152795.1:n.1257+1721T>G