Canonical Allele Identifier: CA1980144145
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483236G= , CM000673.2:g.67483236G= GRCh38
NC_000011.9:g.67250707G= , CM000673.1:g.67250707G= GRCh37
NC_000011.8:g.67007283G= NCBI36
NG_008969.1:g.5203G= , LRG_460:g.5203G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.55G=
ENST00000528641.7:c.78G= ENSP00000434982.3:p.Pro26=
ENST00000529797.2:n.8G=
ENST00000682324.1:c.78G= ENSP00000508017.1:p.Pro26=
ENST00000682659.1:c.78G= ENSP00000507351.1:p.Pro26=
ENST00000682699.1:c.78G= ENSP00000507935.1:p.Pro26=
ENST00000683237.1:c.78G= ENSP00000507343.1:p.Pro26=
ENST00000684006.1:c.78G= ENSP00000507269.1:p.Pro26=
ENST00000684657.1:c.78G= ENSP00000507961.1:p.Pro26=
ENST00000279146.8:c.78G= MANE Select ENSP00000279146.3:p.Pro26=
ENST00000279146.7:c.78G= ENSP00000279146.3:p.Pro26=
ENST00000528641.6:c.78G= ENSP00000434982.2:p.Pro26=
ENST00000529797.1:n.188G=
NM_001302960.1:c.78G= NP_001289889.1:p.Pro26=
NM_003977.3:c.78G= NP_003968.3:p.Pro26=
XM_024448761.1:c.78G= XP_024304529.1:p.Pro26=
NM_003977.4:c.78G= MANE Select NP_003968.3:p.Pro26=
NM_001302960.2:c.78G= NP_001289889.1:p.Pro26=