Canonical Allele Identifier: CA1980172346
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490210T= , CM000673.2:g.67490210T= GRCh38
NC_000011.9:g.67257681T= , CM000673.1:g.67257681T= GRCh37
NC_000011.8:g.67014257T= NCBI36
NG_008969.1:g.12177T= , LRG_460:g.12177T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.618T=
ENST00000528641.7:c.452T= ENSP00000434982.3:p.Met151=
ENST00000529797.2:n.1153T=
ENST00000682324.1:c.468+755T= ENSP00000508017.1:n.468+755T=
ENST00000682659.1:c.272T= ENSP00000507351.1:p.Met91=
ENST00000682699.1:c.641T= ENSP00000507935.1:p.Met214=
ENST00000683237.1:c.641T= ENSP00000507343.1:p.Met214=
ENST00000683856.1:c.464T= ENSP00000507979.1:p.Met155=
ENST00000684006.1:c.641T= ENSP00000507269.1:p.Met214=
ENST00000684657.1:c.461T= ENSP00000507961.1:p.Met154=
ENST00000279146.8:c.641T= MANE Select ENSP00000279146.3:p.Met214=
ENST00000279146.7:c.641T= ENSP00000279146.3:p.Met214=
ENST00000525341.1:c.293T= ENSP00000476993.1:p.Met98=
ENST00000528641.6:c.452T= ENSP00000434982.2:p.Met151=
NM_001302959.1:c.464T= NP_001289888.1:p.Met155=
NM_001302960.1:c.641T= NP_001289889.1:p.Met214=
NM_003977.3:c.641T= NP_003968.3:p.Met214=
XM_024448761.1:c.641T= XP_024304529.1:p.Met214=
NM_003977.4:c.641T= MANE Select NP_003968.3:p.Met214=
NM_001302960.2:c.641T= NP_001289889.1:p.Met214=
NM_001302959.2:c.464T= NP_001289888.1:p.Met155=