Canonical Allele Identifier: CA1980170066
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483039T= , CM000673.2:g.67483039T= GRCh38
NC_000011.9:g.67250510T= , CM000673.1:g.67250510T= GRCh37
NC_000011.8:g.67007086T= NCBI36
NG_008969.1:g.5006T= , LRG_460:g.5006T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-120T= ENSP00000507935.1:n.-120T=
ENST00000279146.8:c.-120T= MANE Select ENSP00000279146.3:n.-120T=
NM_001302960.1:c.-120T= NP_001289889.1:n.-120T=
NM_003977.3:c.-120T= NP_003968.3:n.-120T=
XM_024448761.1:c.-120T= XP_024304529.1:n.-120T=
NM_003977.4:c.-120T= MANE Select NP_003968.3:n.-120T=
NM_001302960.2:c.-120T= NP_001289889.1:n.-120T=