Canonical Allele Identifier: CA381554498
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490817A>T , CM000673.2:g.67490817A>T GRCh38
NC_000011.9:g.67258288A>T , CM000673.1:g.67258288A>T GRCh37
NC_000011.8:g.67014864A>T NCBI36
NG_008969.1:g.12784A>T , LRG_460:g.12784A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.1124A>T
ENST00000528641.7:c.628A>T ENSP00000434982.3:p.Lys210Ter
ENST00000529797.2:n.1659A>T
ENST00000682324.1:c.469-180A>T ENSP00000508017.1:n.469-180A>T
ENST00000682659.1:c.448A>T ENSP00000507351.1:p.Lys150Ter
ENST00000682699.1:c.817A>T ENSP00000507935.1:p.Lys273Ter
ENST00000683237.1:c.809A>T ENSP00000507343.1:p.Gln270Leu
ENST00000683856.1:c.640A>T ENSP00000507979.1:p.Lys214Ter
ENST00000684006.1:c.806A>T ENSP00000507269.1:p.Gln269Leu
ENST00000684657.1:c.637A>T ENSP00000507961.1:p.Lys213Ter
ENST00000279146.8:c.817A>T MANE Select ENSP00000279146.3:p.Lys273Ter
ENST00000279146.7:c.817A>T ENSP00000279146.3:p.Lys273Ter
ENST00000528641.6:c.628A>T ENSP00000434982.2:p.Lys210Ter
NM_001302959.1:c.640A>T NP_001289888.1:p.Lys214Ter
NM_001302960.1:c.809A>T NP_001289889.1:p.Gln270Leu
NM_003977.3:c.817A>T NP_003968.3:p.Lys273Ter
XM_024448761.1:c.817A>T XP_024304529.1:p.Lys273Ter
NM_003977.4:c.817A>T MANE Select NP_003968.3:p.Lys273Ter
NM_001302960.2:c.809A>T NP_001289889.1:p.Gln270Leu
NM_001302959.2:c.640A>T NP_001289888.1:p.Lys214Ter