Canonical Allele Identifier: CA1980172507

Gene: AIP

Linked Data

• dbSNP Id: rs1865885722
• gnomAD v4: 11-67490515-CCTGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490517_67490520del , CM000673.2:g.67490517_67490520del	GRCh38
NC_000011.9:g.67257988_67257991del , CM000673.1:g.67257988_67257991del	GRCh37
NC_000011.8:g.67014564_67014567del	NCBI36
NG_008969.1:g.12484_12487del , LRG_460:g.12484_12487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.824_827del
ENST00000528641.7:c.598+60_598+63del	ENSP00000434982.3:n.598+60_598+63del
ENST00000529797.2:n.1359_1362del
ENST00000682324.1:c.469-480_469-477del	ENSP00000508017.1:n.469-480_469-477del
ENST00000682659.1:c.418+60_418+63del	ENSP00000507351.1:n.418+60_418+63del
ENST00000682699.1:c.787+60_787+63del	ENSP00000507935.1:n.787+60_787+63del
ENST00000683237.1:c.779+68_779+71del	ENSP00000507343.1:n.779+68_779+71del
ENST00000683856.1:c.610+60_610+63del	ENSP00000507979.1:n.610+60_610+63del
ENST00000684006.1:c.787+60_787+63del	ENSP00000507269.1:n.787+60_787+63del
ENST00000684657.1:c.607+60_607+63del	ENSP00000507961.1:n.607+60_607+63del
ENST00000279146.8:c.787+60_787+63del MANE Select	ENSP00000279146.3:n.787+60_787+63del
ENST00000279146.7:c.787+60_787+63del	ENSP00000279146.3:n.787+60_787+63del
ENST00000525341.1:c.499_502del	ENSP00000476993.1:p.Cys167ThrfsTer7
ENST00000528641.6:c.598+60_598+63del	ENSP00000434982.2:n.598+60_598+63del
NM_001302959.1:c.610+60_610+63del	NP_001289888.1:n.610+60_610+63del
NM_001302960.1:c.779+68_779+71del	NP_001289889.1:n.779+68_779+71del
NM_003977.3:c.787+60_787+63del	NP_003968.3:n.787+60_787+63del
XM_024448761.1:c.787+60_787+63del	XP_024304529.1:n.787+60_787+63del
NM_003977.4:c.787+60_787+63del MANE Select	NP_003968.3:n.787+60_787+63del
NM_001302960.2:c.779+68_779+71del	NP_001289889.1:n.779+68_779+71del
NM_001302959.2:c.610+60_610+63del	NP_001289888.1:n.610+60_610+63del