Canonical Allele Identifier: CA1980172335
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490181T= , CM000673.2:g.67490181T= GRCh38
NC_000011.9:g.67257652T= , CM000673.1:g.67257652T= GRCh37
NC_000011.8:g.67014228T= NCBI36
NG_008969.1:g.12148T= , LRG_460:g.12148T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.589T=
ENST00000528641.7:c.423T= ENSP00000434982.3:p.Asp141=
ENST00000529797.2:n.1124T=
ENST00000682324.1:c.468+726T= ENSP00000508017.1:n.468+726T=
ENST00000682659.1:c.243T= ENSP00000507351.1:p.Asp81=
ENST00000682699.1:c.612T= ENSP00000507935.1:p.Asp204=
ENST00000683237.1:c.612T= ENSP00000507343.1:p.Asp204=
ENST00000683856.1:c.435T= ENSP00000507979.1:p.Asp145=
ENST00000684006.1:c.612T= ENSP00000507269.1:p.Asp204=
ENST00000684657.1:c.432T= ENSP00000507961.1:p.Asp144=
ENST00000279146.8:c.612T= MANE Select ENSP00000279146.3:p.Asp204=
ENST00000279146.7:c.612T= ENSP00000279146.3:p.Asp204=
ENST00000525341.1:c.264T= ENSP00000476993.1:p.Asp88=
ENST00000528641.6:c.423T= ENSP00000434982.2:p.Asp141=
NM_001302959.1:c.435T= NP_001289888.1:p.Asp145=
NM_001302960.1:c.612T= NP_001289889.1:p.Asp204=
NM_003977.3:c.612T= NP_003968.3:p.Asp204=
XM_024448761.1:c.612T= XP_024304529.1:p.Asp204=
NM_003977.4:c.612T= MANE Select NP_003968.3:p.Asp204=
NM_001302960.2:c.612T= NP_001289889.1:p.Asp204=
NM_001302959.2:c.435T= NP_001289888.1:p.Asp145=