Canonical Allele Identifier: CA6140922

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490403G>A , CM000673.2:g.67490403G>A	GRCh38
NC_000011.9:g.67257874G>A , CM000673.1:g.67257874G>A	GRCh37
NC_000011.8:g.67014450G>A	NCBI36
NG_008969.1:g.12370G>A , LRG_460:g.12370G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.733G>A MANE Select	NP_003968.3:p.Glu245Lys
ENST00000279146.8:c.733G>A MANE Select	ENSP00000279146.3:p.Glu245Lys
NM_001302959.1:c.556G>A	NP_001289888.1:p.Glu186Lys
NM_001302959.2:c.556G>A	NP_001289888.1:p.Glu186Lys
NM_001302960.1:c.733G>A	NP_001289889.1:p.Glu245Lys
NM_001302960.2:c.733G>A	NP_001289889.1:p.Glu245Lys
NM_003977.3:c.733G>A	NP_003968.3:p.Glu245Lys
ENST00000279146.7:c.733G>A	ENSP00000279146.3:p.Glu245Lys
ENST00000525341.1:c.385G>A	ENSP00000476993.1:p.Glu129Lys
ENST00000525341.2:c.710G>A
ENST00000528641.6:c.544G>A	ENSP00000434982.2:p.Glu182Lys
ENST00000528641.7:c.544G>A	ENSP00000434982.3:p.Glu182Lys
ENST00000529797.2:n.1245G>A
ENST00000682324.1:c.469-594G>A	ENSP00000508017.1:n.469-594G>A
ENST00000682659.1:c.364G>A	ENSP00000507351.1:p.Glu122Lys
ENST00000682699.1:c.733G>A	ENSP00000507935.1:p.Glu245Lys
ENST00000683237.1:c.733G>A	ENSP00000507343.1:p.Glu245Lys
ENST00000683856.1:c.556G>A	ENSP00000507979.1:p.Glu186Lys
ENST00000684006.1:c.733G>A	ENSP00000507269.1:p.Glu245Lys
ENST00000684657.1:c.553G>A	ENSP00000507961.1:p.Glu185Lys
XM_024448761.1:c.733G>A	XP_024304529.1:p.Glu245Lys