Canonical Allele Identifier: CA2742722767

Gene: PLA2G2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978282_19978283insCGCCCATCAGGAACCGGCACTGTCTTTGCAGCTCCC , CM000663.2:g.19978282_19978283insCGCCCATCAGGAACCGGCACTGTCTTTGCAGCTCCC	GRCh38
NC_000001.10:g.20304775_20304776insCGCCCATCAGGAACCGGCACTGTCTTTGCAGCTCCC , CM000663.1:g.20304775_20304776insCGCCCATCAGGAACCGGCACTGTCTTTGCAGCTCCC	GRCh37
NC_000001.9:g.20177362_20177363insCGCCCATCAGGAACCGGCACTGTCTTTGCAGCTCCC	NCBI36
NG_012928.1:g.7157_7158insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG MANE Select	ENSP00000504762.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTT...
ENST00000400520.8:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	ENSP00000383364.3:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTT...
ENST00000482011.2:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	ENSP00000504762.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTT...
ENST00000649436.1:c.104+97_104+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	ENSP00000496912.1:n.104+97_104+98insGGGAGCTGCAAAGACAGTGCCGGTT...
ENST00000375111.7:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	ENSP00000364252.3:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTT...
ENST00000400520.7:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	ENSP00000383364.3:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTT...
ENST00000461140.1:n.536_537insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG
ENST00000469162.5:n.351+97_351+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG
ENST00000482011.1:n.457+97_457+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG
ENST00000491964.5:n.417+97_417+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG
ENST00000496748.1:n.632_633insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG
NM_000300.3:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	NP_000291.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGAT...
NM_001161727.1:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	NP_001155199.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCT...
NM_001161728.1:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	NP_001155200.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCT...
NM_001161729.1:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	NP_001155201.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCT...
NM_000300.4:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	NP_000291.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGAT...
NM_001161727.2:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	NP_001155199.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCT...
NM_001161728.2:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG	NP_001155200.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCT...
NM_001395463.1:c.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCTGATGGGCG MANE Select	NP_001382392.1:n.185+97_185+98insGGGAGCTGCAAAGACAGTGCCGGTTCCT...