Canonical Allele Identifier: CA344052

Gene: AIP

Linked Data

• ClinVar Variation Id: 41158
• ClinVar RCV Id: RCV000034057
• MyVariant Identifiers: chr11:g.67249418_67255234del (hg19) ; chr11:g.67481947_67487763del (hg38)
• PubMed: PMID:22720333

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67481947_67487763del , CM000673.2:g.67481947_67487763del	GRCh38
NC_000011.9:g.67249418_67255234del , CM000673.1:g.67249418_67255234del	GRCh37
NC_000011.8:g.67005994_67011810del	NCBI36
NG_008969.1:g.3914_9730del , LRG_460:g.3914_9730del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682699.1:c.-366-846_279+578del
XM_024448761.1:c.-366-846_279+578del