Canonical Allele Identifier: CA381551298
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490200A>C , CM000673.2:g.67490200A>C GRCh38
NC_000011.9:g.67257671A>C , CM000673.1:g.67257671A>C GRCh37
NC_000011.8:g.67014247A>C NCBI36
NG_008969.1:g.12167A>C , LRG_460:g.12167A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.608A>C
ENST00000528641.7:c.442A>C ENSP00000434982.3:p.Asn148His
ENST00000529797.2:n.1143A>C
ENST00000682324.1:c.468+745A>C ENSP00000508017.1:n.468+745A>C
ENST00000682659.1:c.262A>C ENSP00000507351.1:p.Asn88His
ENST00000682699.1:c.631A>C ENSP00000507935.1:p.Asn211His
ENST00000683237.1:c.631A>C ENSP00000507343.1:p.Asn211His
ENST00000683856.1:c.454A>C ENSP00000507979.1:p.Asn152His
ENST00000684006.1:c.631A>C ENSP00000507269.1:p.Asn211His
ENST00000684657.1:c.451A>C ENSP00000507961.1:p.Asn151His
ENST00000279146.8:c.631A>C MANE Select ENSP00000279146.3:p.Asn211His
ENST00000279146.7:c.631A>C ENSP00000279146.3:p.Asn211His
ENST00000525341.1:c.283A>C ENSP00000476993.1:p.Asn95His
ENST00000528641.6:c.442A>C ENSP00000434982.2:p.Asn148His
NM_001302959.1:c.454A>C NP_001289888.1:p.Asn152His
NM_001302960.1:c.631A>C NP_001289889.1:p.Asn211His
NM_003977.3:c.631A>C NP_003968.3:p.Asn211His
XM_024448761.1:c.631A>C XP_024304529.1:p.Asn211His
NM_003977.4:c.631A>C MANE Select NP_003968.3:p.Asn211His
NM_001302960.2:c.631A>C NP_001289889.1:p.Asn211His
NM_001302959.2:c.454A>C NP_001289888.1:p.Asn152His