Canonical Allele Identifier: CA356563

Gene: AIP

Linked Data

• dbSNP Id: rs267606583
• MyVariant Identifiers: chr11:g.67258349_67258350delinsGT (hg19) ; chr11:g.67490878_67490879delinsGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490878_67490879delinsGT , CM000673.2:g.67490878_67490879delinsGT	GRCh38
NC_000011.9:g.67258349_67258350delinsGT , CM000673.1:g.67258349_67258350delinsGT	GRCh37
NC_000011.8:g.67014925_67014926delinsGT	NCBI36
NG_008969.1:g.12845_12846delinsGT , LRG_460:g.12845_12846delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1185_1186delinsGT
ENST00000528641.7:c.689_690delinsGT	ENSP00000434982.3:p.Glu230Gly
ENST00000529797.2:n.1720_1721delinsGT
ENST00000682324.1:c.469-119_469-118delinsGT	ENSP00000508017.1:n.469-119_469-118delinsGT
ENST00000682659.1:c.509_510delinsGT	ENSP00000507351.1:p.Glu170Gly
ENST00000682699.1:c.878_879delinsGT	ENSP00000507935.1:p.Glu293Gly
ENST00000683237.1:c.*18_*19delinsGT	ENSP00000507343.1:n.*18_*19delinsGT
ENST00000683856.1:c.701_702delinsGT	ENSP00000507979.1:p.Glu234Gly
ENST00000684006.1:c.*18_*19delinsGT	ENSP00000507269.1:n.*18_*19delinsGT
ENST00000684657.1:c.698_699delinsGT	ENSP00000507961.1:p.Glu233Gly
ENST00000279146.8:c.878_879delinsGT MANE Select	ENSP00000279146.3:p.Glu293Gly
ENST00000279146.7:c.878_879delinsGT	ENSP00000279146.3:p.Glu293Gly
ENST00000528641.6:c.689_690delinsGT	ENSP00000434982.2:p.Glu230Gly
NM_001302959.1:c.701_702delinsGT	NP_001289888.1:p.Glu234Gly
NM_001302960.1:c.*18_*19delinsGT	NP_001289889.1:n.*18_*19delinsGT
NM_003977.3:c.878_879delinsGT	NP_003968.3:p.Glu293Gly
XM_024448761.1:c.878_879delinsGT	XP_024304529.1:p.Glu293Gly
NM_003977.4:c.878_879delinsGT MANE Select	NP_003968.3:p.Glu293Gly
NM_001302960.2:c.*18_*19delinsGT	NP_001289889.1:n.*18_*19delinsGT
NM_001302959.2:c.701_702delinsGT	NP_001289888.1:p.Glu234Gly