Canonical Allele Identifier: CA1980170122
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483123C= , CM000673.2:g.67483123C= GRCh38
NC_000011.9:g.67250594C= , CM000673.1:g.67250594C= GRCh37
NC_000011.8:g.67007170C= NCBI36
NG_008969.1:g.5090C= , LRG_460:g.5090C=

Transcript Alleles

HGVS Amino-acid change
ENST00000528641.7:c.-36C= ENSP00000434982.3:n.-36C=
ENST00000682324.1:c.-36C= ENSP00000508017.1:n.-36C=
ENST00000682699.1:c.-36C= ENSP00000507935.1:n.-36C=
ENST00000683237.1:c.-36C= ENSP00000507343.1:n.-36C=
ENST00000684006.1:c.-36C= ENSP00000507269.1:n.-36C=
ENST00000684657.1:c.-36C= ENSP00000507961.1:n.-36C=
ENST00000279146.8:c.-36C= MANE Select ENSP00000279146.3:n.-36C=
ENST00000279146.7:c.-36C= ENSP00000279146.3:n.-36C=
ENST00000528641.6:c.-36C= ENSP00000434982.2:n.-36C=
ENST00000529797.1:n.75C=
NM_001302960.1:c.-36C= NP_001289889.1:n.-36C=
NM_003977.3:c.-36C= NP_003968.3:n.-36C=
XM_024448761.1:c.-36C= XP_024304529.1:n.-36C=
NM_003977.4:c.-36C= MANE Select NP_003968.3:n.-36C=
NM_001302960.2:c.-36C= NP_001289889.1:n.-36C=