Canonical Allele Identifier: CA2614627307

Gene: AIP

Linked Data

• gnomAD v4: 11-67491016-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67491016A>T , CM000673.2:g.67491016A>T	GRCh38
NC_000011.9:g.67258487A>T , CM000673.1:g.67258487A>T	GRCh37
NC_000011.8:g.67015063A>T	NCBI36
NG_008969.1:g.12983A>T , LRG_460:g.12983A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.*23A>T	ENSP00000434982.3:n.*23A>T
ENST00000529797.2:n.1858A>T
ENST00000682324.1:c.488A>T	ENSP00000508017.1:p.Tyr163Phe
ENST00000682659.1:c.*23A>T	ENSP00000507351.1:n.*23A>T
ENST00000683237.1:c.*156A>T	ENSP00000507343.1:n.*156A>T
ENST00000683856.1:c.*23A>T	ENSP00000507979.1:n.*23A>T
ENST00000684006.1:c.*156A>T	ENSP00000507269.1:n.*156A>T
ENST00000684657.1:c.*23A>T	ENSP00000507961.1:n.*23A>T
ENST00000279146.8:c.*23A>T MANE Select	ENSP00000279146.3:n.*23A>T
ENST00000279146.7:c.*23A>T	ENSP00000279146.3:n.*23A>T
NM_001302959.1:c.*23A>T	NP_001289888.1:n.*23A>T
NM_001302960.1:c.*156A>T	NP_001289889.1:n.*156A>T
NM_003977.3:c.*23A>T	NP_003968.3:n.*23A>T
XM_024448761.1:c.*23A>T	XP_024304529.1:n.*23A>T
NM_003977.4:c.*23A>T MANE Select	NP_003968.3:n.*23A>T
NM_001302960.2:c.*156A>T	NP_001289889.1:n.*156A>T
NM_001302959.2:c.*23A>T	NP_001289888.1:n.*23A>T