Canonical Allele Identifier: CA1980170063
Gene: AIP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483031T= , CM000673.2:g.67483031T= GRCh38
NC_000011.9:g.67250502T= , CM000673.1:g.67250502T= GRCh37
NC_000011.8:g.67007078T= NCBI36
NG_008969.1:g.4998T= , LRG_460:g.4998T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-128T= ENSP00000507935.1:n.-128T=
ENST00000279146.8:c.-128T= MANE Select ENSP00000279146.3:n.-128T=
NM_001302960.1:c.-128T= NP_001289889.1:n.-128T=
NM_003977.3:c.-128T= NP_003968.3:n.-128T=
XM_024448761.1:c.-128T= XP_024304529.1:n.-128T=
NM_003977.4:c.-128T= MANE Select NP_003968.3:n.-128T=
NM_001302960.2:c.-128T= NP_001289889.1:n.-128T=
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