Canonical Allele Identifier: CA2614623341

Gene: AIP

Linked Data

• gnomAD v4: 11-67490180-ATGCCATTGCCTGCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490181_67490195del , CM000673.2:g.67490181_67490195del	GRCh38
NC_000011.9:g.67257652_67257666del , CM000673.1:g.67257652_67257666del	GRCh37
NC_000011.8:g.67014228_67014242del	NCBI36
NG_008969.1:g.12148_12162del , LRG_460:g.12148_12162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.589_603del
ENST00000528641.7:c.423_437del	ENSP00000434982.3:p.Ala142_Leu146del
ENST00000529797.2:n.1124_1138del
ENST00000682324.1:c.468+726_468+740del	ENSP00000508017.1:n.468+726_468+740del
ENST00000682659.1:c.243_257del	ENSP00000507351.1:p.Ala82_Leu86del
ENST00000682699.1:c.612_626del	ENSP00000507935.1:p.Ala205_Leu209del
ENST00000683237.1:c.612_626del	ENSP00000507343.1:p.Ala205_Leu209del
ENST00000683856.1:c.435_449del	ENSP00000507979.1:p.Ala146_Leu150del
ENST00000684006.1:c.612_626del	ENSP00000507269.1:p.Ala205_Leu209del
ENST00000684657.1:c.432_446del	ENSP00000507961.1:p.Ala145_Leu149del
ENST00000279146.8:c.612_626del MANE Select	ENSP00000279146.3:p.Ala205_Leu209del
ENST00000279146.7:c.612_626del	ENSP00000279146.3:p.Ala205_Leu209del
ENST00000525341.1:c.264_278del	ENSP00000476993.1:p.Ala89_Leu93del
ENST00000528641.6:c.423_437del	ENSP00000434982.2:p.Ala142_Leu146del
NM_001302959.1:c.435_449del	NP_001289888.1:p.Ala146_Leu150del
NM_001302960.1:c.612_626del	NP_001289889.1:p.Ala205_Leu209del
NM_003977.3:c.612_626del	NP_003968.3:p.Ala205_Leu209del
XM_024448761.1:c.612_626del	XP_024304529.1:p.Ala205_Leu209del
NM_003977.4:c.612_626del MANE Select	NP_003968.3:p.Ala205_Leu209del
NM_001302960.2:c.612_626del	NP_001289889.1:p.Ala205_Leu209del
NM_001302959.2:c.435_449del	NP_001289888.1:p.Ala146_Leu150del