Canonical Allele Identifier: CA1980170126

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483132G= , CM000673.2:g.67483132G=	GRCh38
NC_000011.9:g.67250603G= , CM000673.1:g.67250603G=	GRCh37
NC_000011.8:g.67007179G=	NCBI36
NG_008969.1:g.5099G= , LRG_460:g.5099G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000528641.7:c.-27G=	ENSP00000434982.3:n.-27G=
ENST00000682324.1:c.-27G=	ENSP00000508017.1:n.-27G=
ENST00000682699.1:c.-27G=	ENSP00000507935.1:n.-27G=
ENST00000683237.1:c.-27G=	ENSP00000507343.1:n.-27G=
ENST00000684006.1:c.-27G=	ENSP00000507269.1:n.-27G=
ENST00000684657.1:c.-27G=	ENSP00000507961.1:n.-27G=
ENST00000279146.8:c.-27G= MANE Select	ENSP00000279146.3:n.-27G=
ENST00000279146.7:c.-27G=	ENSP00000279146.3:n.-27G=
ENST00000528641.6:c.-27G=	ENSP00000434982.2:n.-27G=
ENST00000529797.1:n.84G=
NM_001302960.1:c.-27G=	NP_001289889.1:n.-27G=
NM_003977.3:c.-27G=	NP_003968.3:n.-27G=
XM_024448761.1:c.-27G=	XP_024304529.1:n.-27G=
NM_003977.4:c.-27G= MANE Select	NP_003968.3:n.-27G=
NM_001302960.2:c.-27G=	NP_001289889.1:n.-27G=