Canonical Allele Identifier: CA2574896181

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483151del , CM000673.2:g.67483151del	GRCh38
NC_000011.9:g.67250622del , CM000673.1:g.67250622del	GRCh37
NC_000011.8:g.67007198del	NCBI36
NG_008969.1:g.5118del , LRG_460:g.5118del

Transcript Alleles

HGVS	Amino-acid change
ENST00000528641.7:c.-8del	ENSP00000434982.3:n.-8del
ENST00000682324.1:c.-8del	ENSP00000508017.1:n.-8del
ENST00000682699.1:c.-8del	ENSP00000507935.1:n.-8del
ENST00000683237.1:c.-8del	ENSP00000507343.1:n.-8del
ENST00000684006.1:c.-8del	ENSP00000507269.1:n.-8del
ENST00000684657.1:c.-8del	ENSP00000507961.1:n.-8del
ENST00000279146.8:c.-8del MANE Select	ENSP00000279146.3:n.-8del
ENST00000279146.7:c.-8del	ENSP00000279146.3:n.-8del
ENST00000528641.6:c.-8del	ENSP00000434982.2:n.-8del
ENST00000529797.1:n.103del
NM_001302960.1:c.-8del	NP_001289889.1:n.-8del
NM_003977.3:c.-8del	NP_003968.3:n.-8del
XM_024448761.1:c.-8del	XP_024304529.1:n.-8del
NM_003977.4:c.-8del MANE Select	NP_003968.3:n.-8del
NM_001302960.2:c.-8del	NP_001289889.1:n.-8del