Canonical Allele Identifier: CA1980172679

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490879_67490891delinsGCTGGACCCAGCC , CM000673.2:g.67490879_67490891delinsGCTGGACCCAGCC	GRCh38
NC_000011.9:g.67258350_67258362delinsGCTGGACCCAGCC , CM000673.1:g.67258350_67258362delinsGCTGGACCCAGCC	GRCh37
NC_000011.8:g.67014926_67014938delinsGCTGGACCCAGCC	NCBI36
NG_008969.1:g.12846_12858delinsGCTGGACCCAGCC , LRG_460:g.12846_12858delinsGCTGGACCCAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1186_1198delinsGCTGGACCCAGCC
ENST00000528641.7:c.690_702delinsGCTGGACCCAGCC	ENSP00000434982.3:p.Glu230=
ENST00000529797.2:n.1721_1733delinsGCTGGACCCAGCC
ENST00000682324.1:c.469-118_469-106delinsGCTGGACCCAGCC	ENSP00000508017.1:n.469-118_469-106delinsGCTGGACCCAGCC
ENST00000682659.1:c.510_522delinsGCTGGACCCAGCC	ENSP00000507351.1:p.Glu170=
ENST00000682699.1:c.879_891delinsGCTGGACCCAGCC	ENSP00000507935.1:p.Glu293=
ENST00000683237.1:c.*19_*31delinsGCTGGACCCAGCC	ENSP00000507343.1:n.*19_*31delinsGCTGGACCCAGCC
ENST00000683856.1:c.702_714delinsGCTGGACCCAGCC	ENSP00000507979.1:p.Glu234=
ENST00000684006.1:c.*19_*31delinsGCTGGACCCAGCC	ENSP00000507269.1:n.*19_*31delinsGCTGGACCCAGCC
ENST00000684657.1:c.699_711delinsGCTGGACCCAGCC	ENSP00000507961.1:p.Glu233=
ENST00000279146.8:c.879_891delinsGCTGGACCCAGCC MANE Select	ENSP00000279146.3:p.Glu293=
ENST00000279146.7:c.879_891delinsGCTGGACCCAGCC	ENSP00000279146.3:p.Glu293=
NM_001302959.1:c.702_714delinsGCTGGACCCAGCC	NP_001289888.1:p.Glu234=
NM_001302960.1:c.*19_*31delinsGCTGGACCCAGCC	NP_001289889.1:n.*19_*31delinsGCTGGACCCAGCC
NM_003977.3:c.879_891delinsGCTGGACCCAGCC	NP_003968.3:p.Glu293=
XM_024448761.1:c.879_891delinsGCTGGACCCAGCC	XP_024304529.1:p.Glu293=
NM_003977.4:c.879_891delinsGCTGGACCCAGCC MANE Select	NP_003968.3:p.Glu293=
NM_001302960.2:c.*19_*31delinsGCTGGACCCAGCC	NP_001289889.1:n.*19_*31delinsGCTGGACCCAGCC
NM_001302959.2:c.702_714delinsGCTGGACCCAGCC	NP_001289888.1:p.Glu234=