Canonical Allele Identifier: CA1980172275

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490059C= , CM000673.2:g.67490059C=	GRCh38
NC_000011.9:g.67257530C= , CM000673.1:g.67257530C=	GRCh37
NC_000011.8:g.67014106C=	NCBI36
NG_008969.1:g.12026C= , LRG_460:g.12026C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.467C=
ENST00000528641.7:c.301C=	ENSP00000434982.3:p.Gln101=
ENST00000529797.2:n.1002C=
ENST00000682324.1:c.468+604C=	ENSP00000508017.1:n.468+604C=
ENST00000682659.1:c.121C=	ENSP00000507351.1:p.Gln41=
ENST00000682699.1:c.490C=	ENSP00000507935.1:p.Gln164=
ENST00000683237.1:c.490C=	ENSP00000507343.1:p.Gln164=
ENST00000683856.1:c.313C=	ENSP00000507979.1:p.Gln105=
ENST00000684006.1:c.490C=	ENSP00000507269.1:p.Gln164=
ENST00000684657.1:c.310C=	ENSP00000507961.1:p.Gln104=
ENST00000279146.8:c.490C= MANE Select	ENSP00000279146.3:p.Gln164=
ENST00000279146.7:c.490C=	ENSP00000279146.3:p.Gln164=
ENST00000525341.1:c.142C=	ENSP00000476993.1:p.Gln48=
ENST00000528641.6:c.301C=	ENSP00000434982.2:p.Gln101=
NM_001302959.1:c.313C=	NP_001289888.1:p.Gln105=
NM_001302960.1:c.490C=	NP_001289889.1:p.Gln164=
NM_003977.3:c.490C=	NP_003968.3:p.Gln164=
XM_024448761.1:c.490C=	XP_024304529.1:p.Gln164=
NM_003977.4:c.490C= MANE Select	NP_003968.3:p.Gln164=
NM_001302960.2:c.490C=	NP_001289889.1:p.Gln164=
NM_001302959.2:c.313C=	NP_001289888.1:p.Gln105=