Canonical Allele Identifier: CA1980172307
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490124G= , CM000673.2:g.67490124G= GRCh38
NC_000011.9:g.67257595G= , CM000673.1:g.67257595G= GRCh37
NC_000011.8:g.67014171G= NCBI36
NG_008969.1:g.12091G= , LRG_460:g.12091G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.532G=
ENST00000528641.7:c.366G= ENSP00000434982.3:p.Glu122=
ENST00000529797.2:n.1067G=
ENST00000682324.1:c.468+669G= ENSP00000508017.1:n.468+669G=
ENST00000682659.1:c.186G= ENSP00000507351.1:p.Glu62=
ENST00000682699.1:c.555G= ENSP00000507935.1:p.Glu185=
ENST00000683237.1:c.555G= ENSP00000507343.1:p.Glu185=
ENST00000683856.1:c.378G= ENSP00000507979.1:p.Glu126=
ENST00000684006.1:c.555G= ENSP00000507269.1:p.Glu185=
ENST00000684657.1:c.375G= ENSP00000507961.1:p.Glu125=
ENST00000279146.8:c.555G= MANE Select ENSP00000279146.3:p.Glu185=
ENST00000279146.7:c.555G= ENSP00000279146.3:p.Glu185=
ENST00000525341.1:c.207G= ENSP00000476993.1:p.Glu69=
ENST00000528641.6:c.366G= ENSP00000434982.2:p.Glu122=
NM_001302959.1:c.378G= NP_001289888.1:p.Glu126=
NM_001302960.1:c.555G= NP_001289889.1:p.Glu185=
NM_003977.3:c.555G= NP_003968.3:p.Glu185=
XM_024448761.1:c.555G= XP_024304529.1:p.Glu185=
NM_003977.4:c.555G= MANE Select NP_003968.3:p.Glu185=
NM_001302960.2:c.555G= NP_001289889.1:p.Glu185=
NM_001302959.2:c.378G= NP_001289888.1:p.Glu126=