Canonical Allele Identifier: CA1980170922
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67487060G= , CM000673.2:g.67487060G= GRCh38
NC_000011.9:g.67254531G= , CM000673.1:g.67254531G= GRCh37
NC_000011.8:g.67011107G= NCBI36
NG_008969.1:g.9027G= , LRG_460:g.9027G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.131G=
ENST00000528641.7:c.154G= ENSP00000434982.3:p.Asp52=
ENST00000529797.2:n.84G=
ENST00000682324.1:c.154G= ENSP00000508017.1:p.Asp52=
ENST00000682659.1:c.100-2978G= ENSP00000507351.1:n.100-2978G=
ENST00000682699.1:c.154G= ENSP00000507935.1:p.Asp52=
ENST00000683237.1:c.154G= ENSP00000507343.1:p.Asp52=
ENST00000683856.1:c.-24G= ENSP00000507979.1:n.-24G=
ENST00000684006.1:c.154G= ENSP00000507269.1:p.Asp52=
ENST00000684657.1:c.100-2207G= ENSP00000507961.1:n.100-2207G=
ENST00000279146.8:c.154G= MANE Select ENSP00000279146.3:p.Asp52=
ENST00000279146.7:c.154G= ENSP00000279146.3:p.Asp52=
ENST00000528641.6:c.154G= ENSP00000434982.2:p.Asp52=
ENST00000529797.1:n.264G=
NM_001302959.1:c.-24G= NP_001289888.1:n.-24G=
NM_001302960.1:c.154G= NP_001289889.1:p.Asp52=
NM_003977.3:c.154G= NP_003968.3:p.Asp52=
XM_024448761.1:c.154G= XP_024304529.1:p.Asp52=
NM_003977.4:c.154G= MANE Select NP_003968.3:p.Asp52=
NM_001302960.2:c.154G= NP_001289889.1:p.Asp52=
NM_001302959.2:c.-24G= NP_001289888.1:n.-24G=