Canonical Allele Identifier: CA1980171962
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67489369C= , CM000673.2:g.67489369C= GRCh38
NC_000011.9:g.67256840C= , CM000673.1:g.67256840C= GRCh37
NC_000011.8:g.67013416C= NCBI36
NG_008969.1:g.11336C= , LRG_460:g.11336C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.359C=
ENST00000528641.7:c.280-669C= ENSP00000434982.3:n.280-669C=
ENST00000529797.2:n.312C=
ENST00000682324.1:c.382C= ENSP00000508017.1:p.Arg128=
ENST00000682659.1:c.100-669C= ENSP00000507351.1:n.100-669C=
ENST00000682699.1:c.382C= ENSP00000507935.1:p.Arg128=
ENST00000683237.1:c.382C= ENSP00000507343.1:p.Arg128=
ENST00000683856.1:c.205C= ENSP00000507979.1:p.Arg69=
ENST00000684006.1:c.382C= ENSP00000507269.1:p.Arg128=
ENST00000684657.1:c.202C= ENSP00000507961.1:p.Arg68=
ENST00000279146.8:c.382C= MANE Select ENSP00000279146.3:p.Arg128=
ENST00000279146.7:c.382C= ENSP00000279146.3:p.Arg128=
ENST00000525341.1:c.34C= ENSP00000476993.1:p.Arg12=
ENST00000528641.6:c.280-669C= ENSP00000434982.2:n.280-669C=
ENST00000529797.1:n.492C=
NM_001302959.1:c.205C= NP_001289888.1:p.Arg69=
NM_001302960.1:c.382C= NP_001289889.1:p.Arg128=
NM_003977.3:c.382C= NP_003968.3:p.Arg128=
XM_024448761.1:c.382C= XP_024304529.1:p.Arg128=
NM_003977.4:c.382C= MANE Select NP_003968.3:p.Arg128=
NM_001302960.2:c.382C= NP_001289889.1:p.Arg128=
NM_001302959.2:c.205C= NP_001289888.1:p.Arg69=