Canonical Allele Identifier: CA1980172451

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490409T= , CM000673.2:g.67490409T=	GRCh38
NC_000011.9:g.67257880T= , CM000673.1:g.67257880T=	GRCh37
NC_000011.8:g.67014456T=	NCBI36
NG_008969.1:g.12376T= , LRG_460:g.12376T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.716T=
ENST00000528641.7:c.550T=	ENSP00000434982.3:p.Tyr184=
ENST00000529797.2:n.1251T=
ENST00000682324.1:c.469-588T=	ENSP00000508017.1:n.469-588T=
ENST00000682659.1:c.370T=	ENSP00000507351.1:p.Tyr124=
ENST00000682699.1:c.739T=	ENSP00000507935.1:p.Tyr247=
ENST00000683237.1:c.739T=	ENSP00000507343.1:p.Tyr247=
ENST00000683856.1:c.562T=	ENSP00000507979.1:p.Tyr188=
ENST00000684006.1:c.739T=	ENSP00000507269.1:p.Tyr247=
ENST00000684657.1:c.559T=	ENSP00000507961.1:p.Tyr187=
ENST00000279146.8:c.739T= MANE Select	ENSP00000279146.3:p.Tyr247=
ENST00000279146.7:c.739T=	ENSP00000279146.3:p.Tyr247=
ENST00000525341.1:c.391T=	ENSP00000476993.1:p.Tyr131=
ENST00000528641.6:c.550T=	ENSP00000434982.2:p.Tyr184=
NM_001302959.1:c.562T=	NP_001289888.1:p.Tyr188=
NM_001302960.1:c.739T=	NP_001289889.1:p.Tyr247=
NM_003977.3:c.739T=	NP_003968.3:p.Tyr247=
XM_024448761.1:c.739T=	XP_024304529.1:p.Tyr247=
NM_003977.4:c.739T= MANE Select	NP_003968.3:p.Tyr247=
NM_001302960.2:c.739T=	NP_001289889.1:p.Tyr247=
NM_001302959.2:c.562T=	NP_001289888.1:p.Tyr188=