Canonical Allele Identifier: CA1980172237
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67489989C= , CM000673.2:g.67489989C= GRCh38
NC_000011.9:g.67257460C= , CM000673.1:g.67257460C= GRCh37
NC_000011.8:g.67014036C= NCBI36
NG_008969.1:g.11956C= , LRG_460:g.11956C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.446-49C=
ENST00000528641.7:c.280-49C= ENSP00000434982.3:n.280-49C=
ENST00000529797.2:n.932C=
ENST00000682324.1:c.468+534C= ENSP00000508017.1:n.468+534C=
ENST00000682659.1:c.100-49C= ENSP00000507351.1:n.100-49C=
ENST00000682699.1:c.469-49C= ENSP00000507935.1:n.469-49C=
ENST00000683237.1:c.469-49C= ENSP00000507343.1:n.469-49C=
ENST00000683856.1:c.292-49C= ENSP00000507979.1:n.292-49C=
ENST00000684006.1:c.469-49C= ENSP00000507269.1:n.469-49C=
ENST00000684657.1:c.289-49C= ENSP00000507961.1:n.289-49C=
ENST00000279146.8:c.469-49C= MANE Select ENSP00000279146.3:n.469-49C=
ENST00000279146.7:c.469-49C= ENSP00000279146.3:n.469-49C=
ENST00000525341.1:c.121-49C= ENSP00000476993.1:n.121-49C=
ENST00000528641.6:c.280-49C= ENSP00000434982.2:n.280-49C=
NM_001302959.1:c.292-49C= NP_001289888.1:n.292-49C=
NM_001302960.1:c.469-49C= NP_001289889.1:n.469-49C=
NM_003977.3:c.469-49C= NP_003968.3:n.469-49C=
XM_024448761.1:c.469-49C= XP_024304529.1:n.469-49C=
NM_003977.4:c.469-49C= MANE Select NP_003968.3:n.469-49C=
NM_001302960.2:c.469-49C= NP_001289889.1:n.469-49C=
NM_001302959.2:c.292-49C= NP_001289888.1:n.292-49C=