Canonical Allele Identifier: CA2697548770

Gene: AIP

Linked Data

• ClinVar Variation Id: 2770879
• ClinVar RCV Id: RCV003580897

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487188_67487189del , CM000673.2:g.67487188_67487189del	GRCh38
NC_000011.9:g.67254659_67254660del , CM000673.1:g.67254659_67254660del	GRCh37
NC_000011.8:g.67011235_67011236del	NCBI36
NG_008969.1:g.9155_9156del , LRG_460:g.9155_9156del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.256+3_256+4del
ENST00000528641.7:c.279+3_279+4del	ENSP00000434982.3:n.279+3_279+4del
ENST00000529797.2:n.209+3_209+4del
ENST00000682324.1:c.279+3_279+4del	ENSP00000508017.1:n.279+3_279+4del
ENST00000682659.1:c.100-2850_100-2849del	ENSP00000507351.1:n.100-2850_100-2849del
ENST00000682699.1:c.279+3_279+4del	ENSP00000507935.1:n.279+3_279+4del
ENST00000683237.1:c.279+3_279+4del	ENSP00000507343.1:n.279+3_279+4del
ENST00000683856.1:c.102+3_102+4del	ENSP00000507979.1:n.102+3_102+4del
ENST00000684006.1:c.279+3_279+4del	ENSP00000507269.1:n.279+3_279+4del
ENST00000684657.1:c.100-2079_100-2078del	ENSP00000507961.1:n.100-2079_100-2078del
ENST00000279146.8:c.279+3_279+4del MANE Select	ENSP00000279146.3:n.279+3_279+4del
ENST00000279146.7:c.279+3_279+4del	ENSP00000279146.3:n.279+3_279+4del
ENST00000528641.6:c.279+3_279+4del	ENSP00000434982.2:n.279+3_279+4del
ENST00000529797.1:n.389+3_389+4del
NM_001302959.1:c.102+3_102+4del	NP_001289888.1:n.102+3_102+4del
NM_001302960.1:c.279+3_279+4del	NP_001289889.1:n.279+3_279+4del
NM_003977.3:c.279+3_279+4del	NP_003968.3:n.279+3_279+4del
XM_024448761.1:c.279+3_279+4del	XP_024304529.1:n.279+3_279+4del
NM_003977.4:c.279+3_279+4del MANE Select	NP_003968.3:n.279+3_279+4del
NM_001302960.2:c.279+3_279+4del	NP_001289889.1:n.279+3_279+4del
NM_001302959.2:c.102+3_102+4del	NP_001289888.1:n.102+3_102+4del