Canonical Allele Identifier: CA381555373
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490928G>C , CM000673.2:g.67490928G>C GRCh38
NC_000011.9:g.67258399G>C , CM000673.1:g.67258399G>C GRCh37
NC_000011.8:g.67014975G>C NCBI36
NG_008969.1:g.12895G>C , LRG_460:g.12895G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.1235G>C
ENST00000528641.7:c.739G>C ENSP00000434982.3:p.Glu247Gln
ENST00000529797.2:n.1770G>C
ENST00000682324.1:c.469-69G>C ENSP00000508017.1:n.469-69G>C
ENST00000682659.1:c.559G>C ENSP00000507351.1:p.Glu187Gln
ENST00000682699.1:c.928G>C ENSP00000507935.1:p.Glu310Gln
ENST00000683237.1:c.*68G>C ENSP00000507343.1:n.*68G>C
ENST00000683856.1:c.751G>C ENSP00000507979.1:p.Glu251Gln
ENST00000684006.1:c.*68G>C ENSP00000507269.1:n.*68G>C
ENST00000684657.1:c.748G>C ENSP00000507961.1:p.Glu250Gln
ENST00000279146.8:c.928G>C MANE Select ENSP00000279146.3:p.Glu310Gln
ENST00000279146.7:c.928G>C ENSP00000279146.3:p.Glu310Gln
NM_001302959.1:c.751G>C NP_001289888.1:p.Glu251Gln
NM_001302960.1:c.*68G>C NP_001289889.1:n.*68G>C
NM_003977.3:c.928G>C NP_003968.3:p.Glu310Gln
XM_024448761.1:c.928G>C XP_024304529.1:p.Glu310Gln
NM_003977.4:c.928G>C MANE Select NP_003968.3:p.Glu310Gln
NM_001302960.2:c.*68G>C NP_001289889.1:n.*68G>C
NM_001302959.2:c.751G>C NP_001289888.1:p.Glu251Gln