Canonical Allele Identifier: CA1980172472

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490453C= , CM000673.2:g.67490453C=	GRCh38
NC_000011.9:g.67257924C= , CM000673.1:g.67257924C=	GRCh37
NC_000011.8:g.67014500C=	NCBI36
NG_008969.1:g.12420C= , LRG_460:g.12420C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.760C=
ENST00000528641.7:c.594C=	ENSP00000434982.3:p.Tyr198=
ENST00000529797.2:n.1295C=
ENST00000682324.1:c.469-544C=	ENSP00000508017.1:n.469-544C=
ENST00000682659.1:c.414C=	ENSP00000507351.1:p.Tyr138=
ENST00000682699.1:c.783C=	ENSP00000507935.1:p.Tyr261=
ENST00000683237.1:c.779+4C=	ENSP00000507343.1:n.779+4C=
ENST00000683856.1:c.606C=	ENSP00000507979.1:p.Tyr202=
ENST00000684006.1:c.783C=	ENSP00000507269.1:p.Tyr261=
ENST00000684657.1:c.603C=	ENSP00000507961.1:p.Tyr201=
ENST00000279146.8:c.783C= MANE Select	ENSP00000279146.3:p.Tyr261=
ENST00000279146.7:c.783C=	ENSP00000279146.3:p.Tyr261=
ENST00000525341.1:c.435C=	ENSP00000476993.1:p.Tyr145=
ENST00000528641.6:c.594C=	ENSP00000434982.2:p.Tyr198=
NM_001302959.1:c.606C=	NP_001289888.1:p.Tyr202=
NM_001302960.1:c.779+4C=	NP_001289889.1:n.779+4C=
NM_003977.3:c.783C=	NP_003968.3:p.Tyr261=
XM_024448761.1:c.783C=	XP_024304529.1:p.Tyr261=
NM_003977.4:c.783C= MANE Select	NP_003968.3:p.Tyr261=
NM_001302960.2:c.779+4C=	NP_001289889.1:n.779+4C=
NM_001302959.2:c.606C=	NP_001289888.1:p.Tyr202=