Canonical Allele Identifier: CA1980170074

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483054T= , CM000673.2:g.67483054T=	GRCh38
NC_000011.9:g.67250525T= , CM000673.1:g.67250525T=	GRCh37
NC_000011.8:g.67007101T=	NCBI36
NG_008969.1:g.5021T= , LRG_460:g.5021T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000528641.7:c.-105T=	ENSP00000434982.3:n.-105T=
ENST00000682699.1:c.-105T=	ENSP00000507935.1:n.-105T=
ENST00000279146.8:c.-105T= MANE Select	ENSP00000279146.3:n.-105T=
ENST00000279146.7:c.-105T=	ENSP00000279146.3:n.-105T=
ENST00000528641.6:c.-105T=	ENSP00000434982.2:n.-105T=
ENST00000529797.1:n.6T=
NM_001302960.1:c.-105T=	NP_001289889.1:n.-105T=
NM_003977.3:c.-105T=	NP_003968.3:n.-105T=
XM_024448761.1:c.-105T=	XP_024304529.1:n.-105T=
NM_003977.4:c.-105T= MANE Select	NP_003968.3:n.-105T=
NM_001302960.2:c.-105T=	NP_001289889.1:n.-105T=