Canonical Allele Identifier: CA1980170070

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483050A= , CM000673.2:g.67483050A=	GRCh38
NC_000011.9:g.67250521A= , CM000673.1:g.67250521A=	GRCh37
NC_000011.8:g.67007097A=	NCBI36
NG_008969.1:g.5017A= , LRG_460:g.5017A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.-109A=	ENSP00000434982.3:n.-109A=
ENST00000682699.1:c.-109A=	ENSP00000507935.1:n.-109A=
ENST00000279146.8:c.-109A= MANE Select	ENSP00000279146.3:n.-109A=
ENST00000279146.7:c.-109A=	ENSP00000279146.3:n.-109A=
ENST00000528641.6:c.-109A=	ENSP00000434982.2:n.-109A=
ENST00000529797.1:n.2A=
NM_001302960.1:c.-109A=	NP_001289889.1:n.-109A=
NM_003977.3:c.-109A=	NP_003968.3:n.-109A=
XM_024448761.1:c.-109A=	XP_024304529.1:n.-109A=
NM_003977.4:c.-109A= MANE Select	NP_003968.3:n.-109A=
NM_001302960.2:c.-109A=	NP_001289889.1:n.-109A=