Canonical Allele Identifier: CA1980172629
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490771A= , CM000673.2:g.67490771A= GRCh38
NC_000011.9:g.67258242A= , CM000673.1:g.67258242A= GRCh37
NC_000011.8:g.67014818A= NCBI36
NG_008969.1:g.12738A= , LRG_460:g.12738A=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.1078A=
ENST00000528641.7:c.599-17A= ENSP00000434982.3:n.599-17A=
ENST00000529797.2:n.1613A=
ENST00000682324.1:c.469-226A= ENSP00000508017.1:n.469-226A=
ENST00000682659.1:c.419-17A= ENSP00000507351.1:n.419-17A=
ENST00000682699.1:c.788-17A= ENSP00000507935.1:n.788-17A=
ENST00000683237.1:c.780-17A= ENSP00000507343.1:n.780-17A=
ENST00000683856.1:c.611-17A= ENSP00000507979.1:n.611-17A=
ENST00000684006.1:c.788-28A= ENSP00000507269.1:n.788-28A=
ENST00000684657.1:c.608-17A= ENSP00000507961.1:n.608-17A=
ENST00000279146.8:c.788-17A= MANE Select ENSP00000279146.3:n.788-17A=
ENST00000279146.7:c.788-17A= ENSP00000279146.3:n.788-17A=
ENST00000528641.6:c.599-17A= ENSP00000434982.2:n.599-17A=
NM_001302959.1:c.611-17A= NP_001289888.1:n.611-17A=
NM_001302960.1:c.780-17A= NP_001289889.1:n.780-17A=
NM_003977.3:c.788-17A= NP_003968.3:n.788-17A=
XM_024448761.1:c.788-17A= XP_024304529.1:n.788-17A=
NM_003977.4:c.788-17A= MANE Select NP_003968.3:n.788-17A=
NM_001302960.2:c.780-17A= NP_001289889.1:n.780-17A=
NM_001302959.2:c.611-17A= NP_001289888.1:n.611-17A=