Canonical Allele Identifier: CA2614618461

Gene: AIP

Linked Data

• gnomAD v4: 11-67483194-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483195del , CM000673.2:g.67483195del	GRCh38
NC_000011.9:g.67250666del , CM000673.1:g.67250666del	GRCh37
NC_000011.8:g.67007242del	NCBI36
NG_008969.1:g.5162del , LRG_460:g.5162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.14del
ENST00000528641.7:c.37del	ENSP00000434982.3:p.Ile13SerfsTer5
ENST00000682324.1:c.37del	ENSP00000508017.1:p.Ile13SerfsTer5
ENST00000682659.1:c.37del	ENSP00000507351.1:p.Ile13SerfsTer5
ENST00000682699.1:c.37del	ENSP00000507935.1:p.Ile13SerfsTer5
ENST00000683237.1:c.37del	ENSP00000507343.1:p.Ile13SerfsTer5
ENST00000684006.1:c.37del	ENSP00000507269.1:p.Ile13SerfsTer5
ENST00000684657.1:c.37del	ENSP00000507961.1:p.Ile13SerfsTer5
ENST00000279146.8:c.37del MANE Select	ENSP00000279146.3:p.Ile13SerfsTer5
ENST00000279146.7:c.37del	ENSP00000279146.3:p.Ile13SerfsTer5
ENST00000528641.6:c.37del	ENSP00000434982.2:p.Ile13SerfsTer5
ENST00000529797.1:n.147del
NM_001302960.1:c.37del	NP_001289889.1:p.Ile13SerfsTer5
NM_003977.3:c.37del	NP_003968.3:p.Ile13SerfsTer5
XM_024448761.1:c.37del	XP_024304529.1:p.Ile13SerfsTer5
NM_003977.4:c.37del MANE Select	NP_003968.3:p.Ile13SerfsTer5
NM_001302960.2:c.37del	NP_001289889.1:p.Ile13SerfsTer5