Canonical Allele Identifier: CA1980172334
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490180A= , CM000673.2:g.67490180A= GRCh38
NC_000011.9:g.67257651A= , CM000673.1:g.67257651A= GRCh37
NC_000011.8:g.67014227A= NCBI36
NG_008969.1:g.12147A= , LRG_460:g.12147A=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.588A=
ENST00000528641.7:c.422A= ENSP00000434982.3:p.Asp141=
ENST00000529797.2:n.1123A=
ENST00000682324.1:c.468+725A= ENSP00000508017.1:n.468+725A=
ENST00000682659.1:c.242A= ENSP00000507351.1:p.Asp81=
ENST00000682699.1:c.611A= ENSP00000507935.1:p.Asp204=
ENST00000683237.1:c.611A= ENSP00000507343.1:p.Asp204=
ENST00000683856.1:c.434A= ENSP00000507979.1:p.Asp145=
ENST00000684006.1:c.611A= ENSP00000507269.1:p.Asp204=
ENST00000684657.1:c.431A= ENSP00000507961.1:p.Asp144=
ENST00000279146.8:c.611A= MANE Select ENSP00000279146.3:p.Asp204=
ENST00000279146.7:c.611A= ENSP00000279146.3:p.Asp204=
ENST00000525341.1:c.263A= ENSP00000476993.1:p.Asp88=
ENST00000528641.6:c.422A= ENSP00000434982.2:p.Asp141=
NM_001302959.1:c.434A= NP_001289888.1:p.Asp145=
NM_001302960.1:c.611A= NP_001289889.1:p.Asp204=
NM_003977.3:c.611A= NP_003968.3:p.Asp204=
XM_024448761.1:c.611A= XP_024304529.1:p.Asp204=
NM_003977.4:c.611A= MANE Select NP_003968.3:p.Asp204=
NM_001302960.2:c.611A= NP_001289889.1:p.Asp204=
NM_001302959.2:c.434A= NP_001289888.1:p.Asp145=