Canonical Allele Identifier: CA2614624261

Gene: AIP

Linked Data

• gnomAD v4: 11-67490451-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490452dup , CM000673.2:g.67490452dup	GRCh38
NC_000011.9:g.67257923dup , CM000673.1:g.67257923dup	GRCh37
NC_000011.8:g.67014499dup	NCBI36
NG_008969.1:g.12419dup , LRG_460:g.12419dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.759dup
ENST00000528641.7:c.593dup	ENSP00000434982.3:p.Tyr198Ter
ENST00000529797.2:n.1294dup
ENST00000682324.1:c.469-545dup	ENSP00000508017.1:n.469-545dup
ENST00000682659.1:c.413dup	ENSP00000507351.1:p.Tyr138Ter
ENST00000682699.1:c.782dup	ENSP00000507935.1:p.Tyr261Ter
ENST00000683237.1:c.779+3dup	ENSP00000507343.1:n.779+3dup
ENST00000683856.1:c.605dup	ENSP00000507979.1:p.Tyr202Ter
ENST00000684006.1:c.782dup	ENSP00000507269.1:p.Tyr261Ter
ENST00000684657.1:c.602dup	ENSP00000507961.1:p.Tyr201Ter
ENST00000279146.8:c.782dup MANE Select	ENSP00000279146.3:p.Tyr261Ter
ENST00000279146.7:c.782dup	ENSP00000279146.3:p.Tyr261Ter
ENST00000525341.1:c.434dup	ENSP00000476993.1:p.Tyr145Ter
ENST00000528641.6:c.593dup	ENSP00000434982.2:p.Tyr198Ter
NM_001302959.1:c.605dup	NP_001289888.1:p.Tyr202Ter
NM_001302960.1:c.779+3dup	NP_001289889.1:n.779+3dup
NM_003977.3:c.782dup	NP_003968.3:p.Tyr261Ter
XM_024448761.1:c.782dup	XP_024304529.1:p.Tyr261Ter
NM_003977.4:c.782dup MANE Select	NP_003968.3:p.Tyr261Ter
NM_001302960.2:c.779+3dup	NP_001289889.1:n.779+3dup
NM_001302959.2:c.605dup	NP_001289888.1:p.Tyr202Ter