Canonical Allele Identifier: CA2792512324

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490217_67490251del , CM000673.2:g.67490217_67490251del	GRCh38
NC_000011.9:g.67257688_67257722del , CM000673.1:g.67257688_67257722del	GRCh37
NC_000011.8:g.67014264_67014298del	NCBI36
NG_008969.1:g.12184_12218del , LRG_460:g.12184_12218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.622+3_622+37del
ENST00000528641.7:c.456+3_456+37del	ENSP00000434982.3:n.456+3_456+37del
ENST00000529797.2:n.1157+3_1157+37del
ENST00000682324.1:c.468+762_469-746del	ENSP00000508017.1:n.468+762_469-746del
ENST00000682659.1:c.276+3_276+37del	ENSP00000507351.1:n.276+3_276+37del
ENST00000682699.1:c.645+3_645+37del	ENSP00000507935.1:n.645+3_645+37del
ENST00000683237.1:c.645+3_645+37del	ENSP00000507343.1:n.645+3_645+37del
ENST00000683856.1:c.468+3_468+37del	ENSP00000507979.1:n.468+3_468+37del
ENST00000684006.1:c.645+3_645+37del	ENSP00000507269.1:n.645+3_645+37del
ENST00000684657.1:c.465+3_465+37del	ENSP00000507961.1:n.465+3_465+37del
ENST00000279146.8:c.645+3_645+37del MANE Select	ENSP00000279146.3:n.645+3_645+37del
ENST00000279146.7:c.645+3_645+37del	ENSP00000279146.3:n.645+3_645+37del
ENST00000525341.1:c.297+3_297+37del	ENSP00000476993.1:n.297+3_297+37del
ENST00000528641.6:c.456+3_456+37del	ENSP00000434982.2:n.456+3_456+37del
NM_001302959.1:c.468+3_468+37del	NP_001289888.1:n.468+3_468+37del
NM_001302960.1:c.645+3_645+37del	NP_001289889.1:n.645+3_645+37del
NM_003977.3:c.645+3_645+37del	NP_003968.3:n.645+3_645+37del
XM_024448761.1:c.645+3_645+37del	XP_024304529.1:n.645+3_645+37del
NM_003977.4:c.645+3_645+37del MANE Select	NP_003968.3:n.645+3_645+37del
NM_001302960.2:c.645+3_645+37del	NP_001289889.1:n.645+3_645+37del
NM_001302959.2:c.468+3_468+37del	NP_001289888.1:n.468+3_468+37del