Canonical Allele Identifier: CA1980172638

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490792C= , CM000673.2:g.67490792C=	GRCh38
NC_000011.9:g.67258263C= , CM000673.1:g.67258263C=	GRCh37
NC_000011.8:g.67014839C=	NCBI36
NG_008969.1:g.12759C= , LRG_460:g.12759C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1099C=
ENST00000528641.7:c.603C=	ENSP00000434982.3:p.Asn201=
ENST00000529797.2:n.1634C=
ENST00000682324.1:c.469-205C=	ENSP00000508017.1:n.469-205C=
ENST00000682659.1:c.423C=	ENSP00000507351.1:p.Asn141=
ENST00000682699.1:c.792C=	ENSP00000507935.1:p.Asn264=
ENST00000683237.1:c.784C=	ENSP00000507343.1:p.Arg262=
ENST00000683856.1:c.615C=	ENSP00000507979.1:p.Asn205=
ENST00000684006.1:c.788-7C=	ENSP00000507269.1:n.788-7C=
ENST00000684657.1:c.612C=	ENSP00000507961.1:p.Asn204=
ENST00000279146.8:c.792C= MANE Select	ENSP00000279146.3:p.Asn264=
ENST00000279146.7:c.792C=	ENSP00000279146.3:p.Asn264=
ENST00000528641.6:c.603C=	ENSP00000434982.2:p.Asn201=
NM_001302959.1:c.615C=	NP_001289888.1:p.Asn205=
NM_001302960.1:c.784C=	NP_001289889.1:p.Arg262=
NM_003977.3:c.792C=	NP_003968.3:p.Asn264=
XM_024448761.1:c.792C=	XP_024304529.1:p.Asn264=
NM_003977.4:c.792C= MANE Select	NP_003968.3:p.Asn264=
NM_001302960.2:c.784C=	NP_001289889.1:p.Arg262=
NM_001302959.2:c.615C=	NP_001289888.1:p.Asn205=