Canonical Allele Identifier: CA1980172639
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490793G= , CM000673.2:g.67490793G= GRCh38
NC_000011.9:g.67258264G= , CM000673.1:g.67258264G= GRCh37
NC_000011.8:g.67014840G= NCBI36
NG_008969.1:g.12760G= , LRG_460:g.12760G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.1100G=
ENST00000528641.7:c.604G= ENSP00000434982.3:p.Val202=
ENST00000529797.2:n.1635G=
ENST00000682324.1:c.469-204G= ENSP00000508017.1:n.469-204G=
ENST00000682659.1:c.424G= ENSP00000507351.1:p.Val142=
ENST00000682699.1:c.793G= ENSP00000507935.1:p.Val265=
ENST00000683237.1:c.785G= ENSP00000507343.1:p.Arg262=
ENST00000683856.1:c.616G= ENSP00000507979.1:p.Val206=
ENST00000684006.1:c.788-6G= ENSP00000507269.1:n.788-6G=
ENST00000684657.1:c.613G= ENSP00000507961.1:p.Val205=
ENST00000279146.8:c.793G= MANE Select ENSP00000279146.3:p.Val265=
ENST00000279146.7:c.793G= ENSP00000279146.3:p.Val265=
ENST00000528641.6:c.604G= ENSP00000434982.2:p.Val202=
NM_001302959.1:c.616G= NP_001289888.1:p.Val206=
NM_001302960.1:c.785G= NP_001289889.1:p.Arg262=
NM_003977.3:c.793G= NP_003968.3:p.Val265=
XM_024448761.1:c.793G= XP_024304529.1:p.Val265=
NM_003977.4:c.793G= MANE Select NP_003968.3:p.Val265=
NM_001302960.2:c.785G= NP_001289889.1:p.Arg262=
NM_001302959.2:c.616G= NP_001289888.1:p.Val206=