Canonical Allele Identifier: CA1980144691

Gene: AIP

Linked Data

• dbSNP Id: rs1865730439
• gnomAD v4: 11-67483313-G-GGAGGAGGCCTTAGGCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483318_67483334dup , CM000673.2:g.67483318_67483334dup	GRCh38
NC_000011.9:g.67250789_67250805dup , CM000673.1:g.67250789_67250805dup	GRCh37
NC_000011.8:g.67007365_67007381dup	NCBI36
NG_008969.1:g.5285_5301dup , LRG_460:g.5285_5301dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.76+61_76+77dup
ENST00000528641.7:c.99+61_99+77dup	ENSP00000434982.3:n.99+61_99+77dup
ENST00000529797.2:n.29+61_29+77dup
ENST00000682324.1:c.99+61_99+77dup	ENSP00000508017.1:n.99+61_99+77dup
ENST00000682659.1:c.99+61_99+77dup	ENSP00000507351.1:n.99+61_99+77dup
ENST00000682699.1:c.99+61_99+77dup	ENSP00000507935.1:n.99+61_99+77dup
ENST00000683237.1:c.99+61_99+77dup	ENSP00000507343.1:n.99+61_99+77dup
ENST00000684006.1:c.99+61_99+77dup	ENSP00000507269.1:n.99+61_99+77dup
ENST00000684657.1:c.99+61_99+77dup	ENSP00000507961.1:n.99+61_99+77dup
ENST00000279146.8:c.99+61_99+77dup MANE Select	ENSP00000279146.3:n.99+61_99+77dup
ENST00000279146.7:c.99+61_99+77dup	ENSP00000279146.3:n.99+61_99+77dup
ENST00000528641.6:c.99+61_99+77dup	ENSP00000434982.2:n.99+61_99+77dup
ENST00000529797.1:n.209+61_209+77dup
NM_001302960.1:c.99+61_99+77dup	NP_001289889.1:n.99+61_99+77dup
NM_003977.3:c.99+61_99+77dup	NP_003968.3:n.99+61_99+77dup
XM_024448761.1:c.99+61_99+77dup	XP_024304529.1:n.99+61_99+77dup
NM_003977.4:c.99+61_99+77dup MANE Select	NP_003968.3:n.99+61_99+77dup
NM_001302960.2:c.99+61_99+77dup	NP_001289889.1:n.99+61_99+77dup