Canonical Allele Identifier: CA381550320
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs764344774

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490054C>A , CM000673.2:g.67490054C>A GRCh38
NC_000011.9:g.67257525C>A , CM000673.1:g.67257525C>A GRCh37
NC_000011.8:g.67014101C>A NCBI36
NG_008969.1:g.12021C>A , LRG_460:g.12021C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.462C>A
ENST00000528641.7:c.296C>A ENSP00000434982.3:p.Thr99Lys
ENST00000529797.2:n.997C>A
ENST00000682324.1:c.468+599C>A ENSP00000508017.1:n.468+599C>A
ENST00000682659.1:c.116C>A ENSP00000507351.1:p.Thr39Lys
ENST00000682699.1:c.485C>A ENSP00000507935.1:p.Thr162Lys
ENST00000683237.1:c.485C>A ENSP00000507343.1:p.Thr162Lys
ENST00000683856.1:c.308C>A ENSP00000507979.1:p.Thr103Lys
ENST00000684006.1:c.485C>A ENSP00000507269.1:p.Thr162Lys
ENST00000684657.1:c.305C>A ENSP00000507961.1:p.Thr102Lys
ENST00000279146.8:c.485C>A MANE Select ENSP00000279146.3:p.Thr162Lys
ENST00000279146.7:c.485C>A ENSP00000279146.3:p.Thr162Lys
ENST00000525341.1:c.137C>A ENSP00000476993.1:p.Thr46Lys
ENST00000528641.6:c.296C>A ENSP00000434982.2:p.Thr99Lys
NM_001302959.1:c.308C>A NP_001289888.1:p.Thr103Lys
NM_001302960.1:c.485C>A NP_001289889.1:p.Thr162Lys
NM_003977.3:c.485C>A NP_003968.3:p.Thr162Lys
XM_024448761.1:c.485C>A XP_024304529.1:p.Thr162Lys
NM_003977.4:c.485C>A MANE Select NP_003968.3:p.Thr162Lys
NM_001302960.2:c.485C>A NP_001289889.1:p.Thr162Lys
NM_001302959.2:c.308C>A NP_001289888.1:p.Thr103Lys