Canonical Allele Identifier: CA1980171959
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67489363C= , CM000673.2:g.67489363C= GRCh38
NC_000011.9:g.67256834C= , CM000673.1:g.67256834C= GRCh37
NC_000011.8:g.67013410C= NCBI36
NG_008969.1:g.11330C= , LRG_460:g.11330C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.353C=
ENST00000528641.7:c.280-675C= ENSP00000434982.3:n.280-675C=
ENST00000529797.2:n.306C=
ENST00000682324.1:c.376C= ENSP00000508017.1:p.Gln126=
ENST00000682659.1:c.100-675C= ENSP00000507351.1:n.100-675C=
ENST00000682699.1:c.376C= ENSP00000507935.1:p.Gln126=
ENST00000683237.1:c.376C= ENSP00000507343.1:p.Gln126=
ENST00000683856.1:c.199C= ENSP00000507979.1:p.Gln67=
ENST00000684006.1:c.376C= ENSP00000507269.1:p.Gln126=
ENST00000684657.1:c.196C= ENSP00000507961.1:p.Gln66=
ENST00000279146.8:c.376C= MANE Select ENSP00000279146.3:p.Gln126=
ENST00000279146.7:c.376C= ENSP00000279146.3:p.Gln126=
ENST00000525341.1:c.28C= ENSP00000476993.1:p.Gln10=
ENST00000528641.6:c.280-675C= ENSP00000434982.2:n.280-675C=
ENST00000529797.1:n.486C=
NM_001302959.1:c.199C= NP_001289888.1:p.Gln67=
NM_001302960.1:c.376C= NP_001289889.1:p.Gln126=
NM_003977.3:c.376C= NP_003968.3:p.Gln126=
XM_024448761.1:c.376C= XP_024304529.1:p.Gln126=
NM_003977.4:c.376C= MANE Select NP_003968.3:p.Gln126=
NM_001302960.2:c.376C= NP_001289889.1:p.Gln126=
NM_001302959.2:c.199C= NP_001289888.1:p.Gln67=