Canonical Allele Identifier: CA1980172626
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490767G= , CM000673.2:g.67490767G= GRCh38
NC_000011.9:g.67258238G= , CM000673.1:g.67258238G= GRCh37
NC_000011.8:g.67014814G= NCBI36
NG_008969.1:g.12734G= , LRG_460:g.12734G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.1074G=
ENST00000528641.7:c.599-21G= ENSP00000434982.3:n.599-21G=
ENST00000529797.2:n.1609G=
ENST00000682324.1:c.469-230G= ENSP00000508017.1:n.469-230G=
ENST00000682659.1:c.419-21G= ENSP00000507351.1:n.419-21G=
ENST00000682699.1:c.788-21G= ENSP00000507935.1:n.788-21G=
ENST00000683237.1:c.780-21G= ENSP00000507343.1:n.780-21G=
ENST00000683856.1:c.611-21G= ENSP00000507979.1:n.611-21G=
ENST00000684006.1:c.788-32G= ENSP00000507269.1:n.788-32G=
ENST00000684657.1:c.608-21G= ENSP00000507961.1:n.608-21G=
ENST00000279146.8:c.788-21G= MANE Select ENSP00000279146.3:n.788-21G=
ENST00000279146.7:c.788-21G= ENSP00000279146.3:n.788-21G=
ENST00000528641.6:c.599-21G= ENSP00000434982.2:n.599-21G=
NM_001302959.1:c.611-21G= NP_001289888.1:n.611-21G=
NM_001302960.1:c.780-21G= NP_001289889.1:n.780-21G=
NM_003977.3:c.788-21G= NP_003968.3:n.788-21G=
XM_024448761.1:c.788-21G= XP_024304529.1:n.788-21G=
NM_003977.4:c.788-21G= MANE Select NP_003968.3:n.788-21G=
NM_001302960.2:c.780-21G= NP_001289889.1:n.780-21G=
NM_001302959.2:c.611-21G= NP_001289888.1:n.611-21G=