Canonical Allele Identifier: CA2574896295

Gene: AIP

Linked Data

• gnomAD v4: 11-67490693-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490696del , CM000673.2:g.67490696del	GRCh38
NC_000011.9:g.67258167del , CM000673.1:g.67258167del	GRCh37
NC_000011.8:g.67014743del	NCBI36
NG_008969.1:g.12663del , LRG_460:g.12663del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1003del
ENST00000528641.7:c.599-92del	ENSP00000434982.3:n.599-92del
ENST00000529797.2:n.1538del
ENST00000682324.1:c.469-301del	ENSP00000508017.1:n.469-301del
ENST00000682659.1:c.419-92del	ENSP00000507351.1:n.419-92del
ENST00000682699.1:c.788-92del	ENSP00000507935.1:n.788-92del
ENST00000683237.1:c.780-92del	ENSP00000507343.1:n.780-92del
ENST00000683856.1:c.611-92del	ENSP00000507979.1:n.611-92del
ENST00000684006.1:c.788-103del	ENSP00000507269.1:n.788-103del
ENST00000684657.1:c.608-92del	ENSP00000507961.1:n.608-92del
ENST00000279146.8:c.788-92del MANE Select	ENSP00000279146.3:n.788-92del
ENST00000279146.7:c.788-92del	ENSP00000279146.3:n.788-92del
ENST00000528641.6:c.599-92del	ENSP00000434982.2:n.599-92del
NM_001302959.1:c.611-92del	NP_001289888.1:n.611-92del
NM_001302960.1:c.780-92del	NP_001289889.1:n.780-92del
NM_003977.3:c.788-92del	NP_003968.3:n.788-92del
XM_024448761.1:c.788-92del	XP_024304529.1:n.788-92del
NM_003977.4:c.788-92del MANE Select	NP_003968.3:n.788-92del
NM_001302960.2:c.780-92del	NP_001289889.1:n.780-92del
NM_001302959.2:c.611-92del	NP_001289888.1:n.611-92del