Canonical Allele Identifier: CA1980172801

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67491099C= , CM000673.2:g.67491099C=	GRCh38
NC_000011.9:g.67258570C= , CM000673.1:g.67258570C=	GRCh37
NC_000011.8:g.67015146C=	NCBI36
NG_008969.1:g.13066C= , LRG_460:g.13066C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.*106C=	ENSP00000434982.3:n.*106C=
ENST00000682324.1:c.571C=
ENST00000683237.1:c.*239C=	ENSP00000507343.1:n.*239C=
ENST00000683856.1:c.*106C=	ENSP00000507979.1:n.*106C=
ENST00000684006.1:c.*239C=	ENSP00000507269.1:n.*239C=
ENST00000684657.1:c.*106C=	ENSP00000507961.1:n.*106C=
ENST00000279146.8:c.*106C= MANE Select	ENSP00000279146.3:n.*106C=
ENST00000279146.7:c.*106C=	ENSP00000279146.3:n.*106C=
NM_001302959.1:c.*106C=	NP_001289888.1:n.*106C=
NM_001302960.1:c.*239C=	NP_001289889.1:n.*239C=
NM_003977.3:c.*106C=	NP_003968.3:n.*106C=
XM_024448761.1:c.*106C=	XP_024304529.1:n.*106C=
NM_003977.4:c.*106C= MANE Select	NP_003968.3:n.*106C=
NM_001302960.2:c.*239C=	NP_001289889.1:n.*239C=
NM_001302959.2:c.*106C=	NP_001289888.1:n.*106C=