Canonical Allele Identifier: CA2574896307

Gene: AIP

Linked Data

• dbSNP Id: rs540045132
• gnomAD v4: 11-67490758-ATGCCCAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490768_67490774del , CM000673.2:g.67490768_67490774del	GRCh38
NC_000011.9:g.67258239_67258245del , CM000673.1:g.67258239_67258245del	GRCh37
NC_000011.8:g.67014815_67014821del	NCBI36
NG_008969.1:g.12735_12741del , LRG_460:g.12735_12741del

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1075_1081del
ENST00000528641.7:c.599-20_599-14del	ENSP00000434982.3:n.599-20_599-14del
ENST00000529797.2:n.1610_1616del
ENST00000682324.1:c.469-229_469-223del	ENSP00000508017.1:n.469-229_469-223del
ENST00000682659.1:c.419-20_419-14del	ENSP00000507351.1:n.419-20_419-14del
ENST00000682699.1:c.788-20_788-14del	ENSP00000507935.1:n.788-20_788-14del
ENST00000683237.1:c.780-20_780-14del	ENSP00000507343.1:n.780-20_780-14del
ENST00000683856.1:c.611-20_611-14del	ENSP00000507979.1:n.611-20_611-14del
ENST00000684006.1:c.788-31_788-25del	ENSP00000507269.1:n.788-31_788-25del
ENST00000684657.1:c.608-20_608-14del	ENSP00000507961.1:n.608-20_608-14del
ENST00000279146.8:c.788-20_788-14del MANE Select	ENSP00000279146.3:n.788-20_788-14del
ENST00000279146.7:c.788-20_788-14del	ENSP00000279146.3:n.788-20_788-14del
ENST00000528641.6:c.599-20_599-14del	ENSP00000434982.2:n.599-20_599-14del
NM_001302959.1:c.611-20_611-14del	NP_001289888.1:n.611-20_611-14del
NM_001302960.1:c.780-20_780-14del	NP_001289889.1:n.780-20_780-14del
NM_003977.3:c.788-20_788-14del	NP_003968.3:n.788-20_788-14del
XM_024448761.1:c.788-20_788-14del	XP_024304529.1:n.788-20_788-14del
NM_003977.4:c.788-20_788-14del MANE Select	NP_003968.3:n.788-20_788-14del
NM_001302960.2:c.780-20_780-14del	NP_001289889.1:n.780-20_780-14del
NM_001302959.2:c.611-20_611-14del	NP_001289888.1:n.611-20_611-14del