Canonical Allele Identifier: CA224165732

Gene: AIP

Linked Data

• dbSNP Id: rs923939866
• gnomAD v2: 11-67258185-CATG-C
• gnomAD v3: 11-67490714-CATG-C
• gnomAD v4: 11-67490714-CATG-C
• MyVariant Identifiers: chr11:g.67258186_67258188del (hg19) ; chr11:g.67490715_67490717del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490716_67490718del , CM000673.2:g.67490716_67490718del	GRCh38
NC_000011.9:g.67258187_67258189del , CM000673.1:g.67258187_67258189del	GRCh37
NC_000011.8:g.67014763_67014765del	NCBI36
NG_008969.1:g.12683_12685del , LRG_460:g.12683_12685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1023_1025del
ENST00000528641.7:c.599-72_599-70del	ENSP00000434982.3:n.599-72_599-70del
ENST00000529797.2:n.1558_1560del
ENST00000682324.1:c.469-281_469-279del	ENSP00000508017.1:n.469-281_469-279del
ENST00000682659.1:c.419-72_419-70del	ENSP00000507351.1:n.419-72_419-70del
ENST00000682699.1:c.788-72_788-70del	ENSP00000507935.1:n.788-72_788-70del
ENST00000683237.1:c.780-72_780-70del	ENSP00000507343.1:n.780-72_780-70del
ENST00000683856.1:c.611-72_611-70del	ENSP00000507979.1:n.611-72_611-70del
ENST00000684006.1:c.788-83_788-81del	ENSP00000507269.1:n.788-83_788-81del
ENST00000684657.1:c.608-72_608-70del	ENSP00000507961.1:n.608-72_608-70del
ENST00000279146.8:c.788-72_788-70del MANE Select	ENSP00000279146.3:n.788-72_788-70del
ENST00000279146.7:c.788-72_788-70del	ENSP00000279146.3:n.788-72_788-70del
ENST00000528641.6:c.599-72_599-70del	ENSP00000434982.2:n.599-72_599-70del
NM_001302959.1:c.611-72_611-70del	NP_001289888.1:n.611-72_611-70del
NM_001302960.1:c.780-72_780-70del	NP_001289889.1:n.780-72_780-70del
NM_003977.3:c.788-72_788-70del	NP_003968.3:n.788-72_788-70del
XM_024448761.1:c.788-72_788-70del	XP_024304529.1:n.788-72_788-70del
NM_003977.4:c.788-72_788-70del MANE Select	NP_003968.3:n.788-72_788-70del
NM_001302960.2:c.780-72_780-70del	NP_001289889.1:n.780-72_780-70del
NM_001302959.2:c.611-72_611-70del	NP_001289888.1:n.611-72_611-70del