Canonical Allele Identifier: CA2614625251

Gene: AIP

Linked Data

• gnomAD v4: 11-67490646-GGGGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490654_67490658del , CM000673.2:g.67490654_67490658del	GRCh38
NC_000011.9:g.67258125_67258129del , CM000673.1:g.67258125_67258129del	GRCh37
NC_000011.8:g.67014701_67014705del	NCBI36
NG_008969.1:g.12621_12625del , LRG_460:g.12621_12625del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.961_965del
ENST00000528641.7:c.599-134_599-130del	ENSP00000434982.3:n.599-134_599-130del
ENST00000529797.2:n.1496_1500del
ENST00000682324.1:c.469-343_469-339del	ENSP00000508017.1:n.469-343_469-339del
ENST00000682659.1:c.419-134_419-130del	ENSP00000507351.1:n.419-134_419-130del
ENST00000682699.1:c.788-134_788-130del	ENSP00000507935.1:n.788-134_788-130del
ENST00000683237.1:c.780-134_780-130del	ENSP00000507343.1:n.780-134_780-130del
ENST00000683856.1:c.611-134_611-130del	ENSP00000507979.1:n.611-134_611-130del
ENST00000684006.1:c.788-145_788-141del	ENSP00000507269.1:n.788-145_788-141del
ENST00000684657.1:c.608-134_608-130del	ENSP00000507961.1:n.608-134_608-130del
ENST00000279146.8:c.788-134_788-130del MANE Select	ENSP00000279146.3:n.788-134_788-130del
ENST00000279146.7:c.788-134_788-130del	ENSP00000279146.3:n.788-134_788-130del
ENST00000528641.6:c.599-134_599-130del	ENSP00000434982.2:n.599-134_599-130del
NM_001302959.1:c.611-134_611-130del	NP_001289888.1:n.611-134_611-130del
NM_001302960.1:c.780-134_780-130del	NP_001289889.1:n.780-134_780-130del
NM_003977.3:c.788-134_788-130del	NP_003968.3:n.788-134_788-130del
XM_024448761.1:c.788-134_788-130del	XP_024304529.1:n.788-134_788-130del
NM_003977.4:c.788-134_788-130del MANE Select	NP_003968.3:n.788-134_788-130del
NM_001302960.2:c.780-134_780-130del	NP_001289889.1:n.780-134_780-130del
NM_001302959.2:c.611-134_611-130del	NP_001289888.1:n.611-134_611-130del