Canonical Allele Identifier: CA1980172641

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490802T= , CM000673.2:g.67490802T=	GRCh38
NC_000011.9:g.67258273T= , CM000673.1:g.67258273T=	GRCh37
NC_000011.8:g.67014849T=	NCBI36
NG_008969.1:g.12769T= , LRG_460:g.12769T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1109T=
ENST00000528641.7:c.613T=	ENSP00000434982.3:p.Tyr205=
ENST00000529797.2:n.1644T=
ENST00000682324.1:c.469-195T=	ENSP00000508017.1:n.469-195T=
ENST00000682659.1:c.433T=	ENSP00000507351.1:p.Tyr145=
ENST00000682699.1:c.802T=	ENSP00000507935.1:p.Tyr268=
ENST00000683237.1:c.794T=	ENSP00000507343.1:p.Leu265=
ENST00000683856.1:c.625T=	ENSP00000507979.1:p.Tyr209=
ENST00000684006.1:c.791T=	ENSP00000507269.1:p.Leu264=
ENST00000684657.1:c.622T=	ENSP00000507961.1:p.Tyr208=
ENST00000279146.8:c.802T= MANE Select	ENSP00000279146.3:p.Tyr268=
ENST00000279146.7:c.802T=	ENSP00000279146.3:p.Tyr268=
ENST00000528641.6:c.613T=	ENSP00000434982.2:p.Tyr205=
NM_001302959.1:c.625T=	NP_001289888.1:p.Tyr209=
NM_001302960.1:c.794T=	NP_001289889.1:p.Leu265=
NM_003977.3:c.802T=	NP_003968.3:p.Tyr268=
XM_024448761.1:c.802T=	XP_024304529.1:p.Tyr268=
NM_003977.4:c.802T= MANE Select	NP_003968.3:p.Tyr268=
NM_001302960.2:c.794T=	NP_001289889.1:p.Leu265=
NM_001302959.2:c.625T=	NP_001289888.1:p.Tyr209=