Canonical Allele Identifier: CA2614624483

Gene: AIP

Linked Data

• gnomAD v4: 11-67490479-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490481del , CM000673.2:g.67490481del	GRCh38
NC_000011.9:g.67257952del , CM000673.1:g.67257952del	GRCh37
NC_000011.8:g.67014528del	NCBI36
NG_008969.1:g.12448del , LRG_460:g.12448del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.788del
ENST00000528641.7:c.598+24del	ENSP00000434982.3:n.598+24del
ENST00000529797.2:n.1323del
ENST00000682324.1:c.469-516del	ENSP00000508017.1:n.469-516del
ENST00000682659.1:c.418+24del	ENSP00000507351.1:n.418+24del
ENST00000682699.1:c.787+24del	ENSP00000507935.1:n.787+24del
ENST00000683237.1:c.779+32del	ENSP00000507343.1:n.779+32del
ENST00000683856.1:c.610+24del	ENSP00000507979.1:n.610+24del
ENST00000684006.1:c.787+24del	ENSP00000507269.1:n.787+24del
ENST00000684657.1:c.607+24del	ENSP00000507961.1:n.607+24del
ENST00000279146.8:c.787+24del MANE Select	ENSP00000279146.3:n.787+24del
ENST00000279146.7:c.787+24del	ENSP00000279146.3:n.787+24del
ENST00000525341.1:c.463del	ENSP00000476993.1:p.Arg155GlyfsTer20
ENST00000528641.6:c.598+24del	ENSP00000434982.2:n.598+24del
NM_001302959.1:c.610+24del	NP_001289888.1:n.610+24del
NM_001302960.1:c.779+32del	NP_001289889.1:n.779+32del
NM_003977.3:c.787+24del	NP_003968.3:n.787+24del
XM_024448761.1:c.787+24del	XP_024304529.1:n.787+24del
NM_003977.4:c.787+24del MANE Select	NP_003968.3:n.787+24del
NM_001302960.2:c.779+32del	NP_001289889.1:n.779+32del
NM_001302959.2:c.610+24del	NP_001289888.1:n.610+24del