Canonical Allele Identifier: CA2614625528

Gene: AIP

Linked Data

• gnomAD v4: 11-67490721-GCAGGCAGCTGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490726_67490737del , CM000673.2:g.67490726_67490737del	GRCh38
NC_000011.9:g.67258197_67258208del , CM000673.1:g.67258197_67258208del	GRCh37
NC_000011.8:g.67014773_67014784del	NCBI36
NG_008969.1:g.12693_12704del , LRG_460:g.12693_12704del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1033_1044del
ENST00000528641.7:c.599-62_599-51del	ENSP00000434982.3:n.599-62_599-51del
ENST00000529797.2:n.1568_1579del
ENST00000682324.1:c.469-271_469-260del	ENSP00000508017.1:n.469-271_469-260del
ENST00000682659.1:c.419-62_419-51del	ENSP00000507351.1:n.419-62_419-51del
ENST00000682699.1:c.788-62_788-51del	ENSP00000507935.1:n.788-62_788-51del
ENST00000683237.1:c.780-62_780-51del	ENSP00000507343.1:n.780-62_780-51del
ENST00000683856.1:c.611-62_611-51del	ENSP00000507979.1:n.611-62_611-51del
ENST00000684006.1:c.788-73_788-62del	ENSP00000507269.1:n.788-73_788-62del
ENST00000684657.1:c.608-62_608-51del	ENSP00000507961.1:n.608-62_608-51del
ENST00000279146.8:c.788-62_788-51del MANE Select	ENSP00000279146.3:n.788-62_788-51del
ENST00000279146.7:c.788-62_788-51del	ENSP00000279146.3:n.788-62_788-51del
ENST00000528641.6:c.599-62_599-51del	ENSP00000434982.2:n.599-62_599-51del
NM_001302959.1:c.611-62_611-51del	NP_001289888.1:n.611-62_611-51del
NM_001302960.1:c.780-62_780-51del	NP_001289889.1:n.780-62_780-51del
NM_003977.3:c.788-62_788-51del	NP_003968.3:n.788-62_788-51del
XM_024448761.1:c.788-62_788-51del	XP_024304529.1:n.788-62_788-51del
NM_003977.4:c.788-62_788-51del MANE Select	NP_003968.3:n.788-62_788-51del
NM_001302960.2:c.780-62_780-51del	NP_001289889.1:n.780-62_780-51del
NM_001302959.2:c.611-62_611-51del	NP_001289888.1:n.611-62_611-51del