Canonical Allele Identifier: CA939068743

Gene: AIP

Linked Data

• gnomAD v3: 11-67487295-CTT-C
• gnomAD v4: 11-67487295-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487305_67487306del , CM000673.2:g.67487305_67487306del	GRCh38
NC_000011.9:g.67254776_67254777del , CM000673.1:g.67254776_67254777del	GRCh37
NC_000011.8:g.67011352_67011353del	NCBI36
NG_008969.1:g.9272_9273del , LRG_460:g.9272_9273del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.256+120_256+121del
ENST00000528641.7:c.279+120_279+121del	ENSP00000434982.3:n.279+120_279+121del
ENST00000529797.2:n.209+120_209+121del
ENST00000682324.1:c.279+120_279+121del	ENSP00000508017.1:n.279+120_279+121del
ENST00000682659.1:c.100-2733_100-2732del	ENSP00000507351.1:n.100-2733_100-2732del
ENST00000682699.1:c.279+120_279+121del	ENSP00000507935.1:n.279+120_279+121del
ENST00000683237.1:c.279+120_279+121del	ENSP00000507343.1:n.279+120_279+121del
ENST00000683856.1:c.102+120_102+121del	ENSP00000507979.1:n.102+120_102+121del
ENST00000684006.1:c.279+120_279+121del	ENSP00000507269.1:n.279+120_279+121del
ENST00000684657.1:c.100-1962_100-1961del	ENSP00000507961.1:n.100-1962_100-1961del
ENST00000279146.8:c.279+120_279+121del MANE Select	ENSP00000279146.3:n.279+120_279+121del
ENST00000279146.7:c.279+120_279+121del	ENSP00000279146.3:n.279+120_279+121del
ENST00000528641.6:c.279+120_279+121del	ENSP00000434982.2:n.279+120_279+121del
ENST00000529797.1:n.389+120_389+121del
NM_001302959.1:c.102+120_102+121del	NP_001289888.1:n.102+120_102+121del
NM_001302960.1:c.279+120_279+121del	NP_001289889.1:n.279+120_279+121del
NM_003977.3:c.279+120_279+121del	NP_003968.3:n.279+120_279+121del
XM_024448761.1:c.279+120_279+121del	XP_024304529.1:n.279+120_279+121del
NM_003977.4:c.279+120_279+121del MANE Select	NP_003968.3:n.279+120_279+121del
NM_001302960.2:c.279+120_279+121del	NP_001289889.1:n.279+120_279+121del
NM_001302959.2:c.102+120_102+121del	NP_001289888.1:n.102+120_102+121del