Canonical Allele Identifier: CA340302
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 4889
ClinVar RCV Id: RCV000005167
dbSNP Id: rs267606567
MyVariant Identifiers: chr11:g.67250695_67250700del (hg19) chr11:g.67483224_67483229del (hg38)
PubMed: PMID:17360484 PMID:22720333
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483224_67483229del , CM000673.2:g.67483224_67483229del GRCh38
NC_000011.9:g.67250695_67250700del , CM000673.1:g.67250695_67250700del GRCh37
NC_000011.8:g.67007271_67007276del NCBI36
NG_008969.1:g.5191_5196del , LRG_460:g.5191_5196del

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.43_48del
ENST00000528641.7:c.66_71del ENSP00000434982.3:p.Gly23_Glu24del
ENST00000682324.1:c.66_71del ENSP00000508017.1:p.Gly23_Glu24del
ENST00000682659.1:c.66_71del ENSP00000507351.1:p.Gly23_Glu24del
ENST00000682699.1:c.66_71del ENSP00000507935.1:p.Gly23_Glu24del
ENST00000683237.1:c.66_71del ENSP00000507343.1:p.Gly23_Glu24del
ENST00000684006.1:c.66_71del ENSP00000507269.1:p.Gly23_Glu24del
ENST00000684657.1:c.66_71del ENSP00000507961.1:p.Gly23_Glu24del
ENST00000279146.8:c.66_71del MANE Select ENSP00000279146.3:p.Gly23_Glu24del
ENST00000279146.7:c.66_71del ENSP00000279146.3:p.Gly23_Glu24del
ENST00000528641.6:c.66_71del ENSP00000434982.2:p.Gly23_Glu24del
ENST00000529797.1:n.176_181del
NM_001302960.1:c.66_71del NP_001289889.1:p.Gly23_Glu24del
NM_003977.3:c.66_71del NP_003968.3:p.Gly23_Glu24del
XM_024448761.1:c.66_71del XP_024304529.1:p.Gly23_Glu24del
NM_003977.4:c.66_71del MANE Select NP_003968.3:p.Gly23_Glu24del
NM_001302960.2:c.66_71del NP_001289889.1:p.Gly23_Glu24del
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