Canonical Allele Identifier: CA2614624648

Gene: AIP

Linked Data

• gnomAD v4: 11-67490531-TCAAGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490533_67490538del , CM000673.2:g.67490533_67490538del	GRCh38
NC_000011.9:g.67258004_67258009del , CM000673.1:g.67258004_67258009del	GRCh37
NC_000011.8:g.67014580_67014585del	NCBI36
NG_008969.1:g.12500_12505del , LRG_460:g.12500_12505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.840_845del
ENST00000528641.7:c.598+76_598+81del	ENSP00000434982.3:n.598+76_598+81del
ENST00000529797.2:n.1375_1380del
ENST00000682324.1:c.469-464_469-459del	ENSP00000508017.1:n.469-464_469-459del
ENST00000682659.1:c.418+76_418+81del	ENSP00000507351.1:n.418+76_418+81del
ENST00000682699.1:c.787+76_787+81del	ENSP00000507935.1:n.787+76_787+81del
ENST00000683237.1:c.779+84_779+89del	ENSP00000507343.1:n.779+84_779+89del
ENST00000683856.1:c.610+76_610+81del	ENSP00000507979.1:n.610+76_610+81del
ENST00000684006.1:c.787+76_787+81del	ENSP00000507269.1:n.787+76_787+81del
ENST00000684657.1:c.607+76_607+81del	ENSP00000507961.1:n.607+76_607+81del
ENST00000279146.8:c.787+76_787+81del MANE Select	ENSP00000279146.3:n.787+76_787+81del
ENST00000279146.7:c.787+76_787+81del	ENSP00000279146.3:n.787+76_787+81del
ENST00000525341.1:c.515_520del	ENSP00000476993.1:p.Gln172_Asp173del
ENST00000528641.6:c.598+76_598+81del	ENSP00000434982.2:n.598+76_598+81del
NM_001302959.1:c.610+76_610+81del	NP_001289888.1:n.610+76_610+81del
NM_001302960.1:c.779+84_779+89del	NP_001289889.1:n.779+84_779+89del
NM_003977.3:c.787+76_787+81del	NP_003968.3:n.787+76_787+81del
XM_024448761.1:c.787+76_787+81del	XP_024304529.1:n.787+76_787+81del
NM_003977.4:c.787+76_787+81del MANE Select	NP_003968.3:n.787+76_787+81del
NM_001302960.2:c.779+84_779+89del	NP_001289889.1:n.779+84_779+89del
NM_001302959.2:c.610+76_610+81del	NP_001289888.1:n.610+76_610+81del