Canonical Allele Identifier: CA1980172681
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490885C= , CM000673.2:g.67490885C= GRCh38
NC_000011.9:g.67258356C= , CM000673.1:g.67258356C= GRCh37
NC_000011.8:g.67014932C= NCBI36
NG_008969.1:g.12852C= , LRG_460:g.12852C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.1192C=
ENST00000528641.7:c.696C= ENSP00000434982.3:p.Asp232=
ENST00000529797.2:n.1727C=
ENST00000682324.1:c.469-112C= ENSP00000508017.1:n.469-112C=
ENST00000682659.1:c.516C= ENSP00000507351.1:p.Asp172=
ENST00000682699.1:c.885C= ENSP00000507935.1:p.Asp295=
ENST00000683237.1:c.*25C= ENSP00000507343.1:n.*25C=
ENST00000683856.1:c.708C= ENSP00000507979.1:p.Asp236=
ENST00000684006.1:c.*25C= ENSP00000507269.1:n.*25C=
ENST00000684657.1:c.705C= ENSP00000507961.1:p.Asp235=
ENST00000279146.8:c.885C= MANE Select ENSP00000279146.3:p.Asp295=
ENST00000279146.7:c.885C= ENSP00000279146.3:p.Asp295=
ENST00000528641.6:c.696C= ENSP00000434982.2:p.Asp232=
NM_001302959.1:c.708C= NP_001289888.1:p.Asp236=
NM_001302960.1:c.*25C= NP_001289889.1:n.*25C=
NM_003977.3:c.885C= NP_003968.3:p.Asp295=
XM_024448761.1:c.885C= XP_024304529.1:p.Asp295=
NM_003977.4:c.885C= MANE Select NP_003968.3:p.Asp295=
NM_001302960.2:c.*25C= NP_001289889.1:n.*25C=
NM_001302959.2:c.708C= NP_001289888.1:p.Asp236=