Canonical Allele Identifier: CA2614623597

Gene: AIP

Linked Data

• gnomAD v4: 11-67490318-A-ACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490320_67490322dup , CM000673.2:g.67490320_67490322dup	GRCh38
NC_000011.9:g.67257791_67257793dup , CM000673.1:g.67257791_67257793dup	GRCh37
NC_000011.8:g.67014367_67014369dup	NCBI36
NG_008969.1:g.12287_12289dup , LRG_460:g.12287_12289dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.627_629dup
ENST00000528641.7:c.461_463dup	ENSP00000434982.3:p.Gln154_Pro155insGln
ENST00000529797.2:n.1162_1164dup
ENST00000682324.1:c.469-677_469-675dup	ENSP00000508017.1:n.469-677_469-675dup
ENST00000682659.1:c.281_283dup	ENSP00000507351.1:p.Gln94_Pro95insGln
ENST00000682699.1:c.650_652dup	ENSP00000507935.1:p.Gln217_Pro218insGln
ENST00000683237.1:c.650_652dup	ENSP00000507343.1:p.Gln217_Pro218insGln
ENST00000683856.1:c.473_475dup	ENSP00000507979.1:p.Gln158_Pro159insGln
ENST00000684006.1:c.650_652dup	ENSP00000507269.1:p.Gln217_Pro218insGln
ENST00000684657.1:c.470_472dup	ENSP00000507961.1:p.Gln157_Pro158insGln
ENST00000279146.8:c.650_652dup MANE Select	ENSP00000279146.3:p.Gln217_Pro218insGln
ENST00000279146.7:c.650_652dup	ENSP00000279146.3:p.Gln217_Pro218insGln
ENST00000525341.1:c.302_304dup	ENSP00000476993.1:p.Gln101_Pro102insGln
ENST00000528641.6:c.461_463dup	ENSP00000434982.2:p.Gln154_Pro155insGln
NM_001302959.1:c.473_475dup	NP_001289888.1:p.Gln158_Pro159insGln
NM_001302960.1:c.650_652dup	NP_001289889.1:p.Gln217_Pro218insGln
NM_003977.3:c.650_652dup	NP_003968.3:p.Gln217_Pro218insGln
XM_024448761.1:c.650_652dup	XP_024304529.1:p.Gln217_Pro218insGln
NM_003977.4:c.650_652dup MANE Select	NP_003968.3:p.Gln217_Pro218insGln
NM_001302960.2:c.650_652dup	NP_001289889.1:p.Gln217_Pro218insGln
NM_001302959.2:c.473_475dup	NP_001289888.1:p.Gln158_Pro159insGln