Canonical Allele Identifier: CA1980170070
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483050A= , CM000673.2:g.67483050A= GRCh38
NC_000011.9:g.67250521A= , CM000673.1:g.67250521A= GRCh37
NC_000011.8:g.67007097A= NCBI36
NG_008969.1:g.5017A= , LRG_460:g.5017A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000528641.7:c.-109A= ENSP00000434982.3:n.-109A=
ENST00000682699.1:c.-109A= ENSP00000507935.1:n.-109A=
ENST00000279146.8:c.-109A= MANE Select ENSP00000279146.3:n.-109A=
ENST00000279146.7:c.-109A= ENSP00000279146.3:n.-109A=
ENST00000528641.6:c.-109A= ENSP00000434982.2:n.-109A=
ENST00000529797.1:n.2A=
NM_001302960.1:c.-109A= NP_001289889.1:n.-109A=
NM_003977.3:c.-109A= NP_003968.3:n.-109A=
XM_024448761.1:c.-109A= XP_024304529.1:n.-109A=
NM_003977.4:c.-109A= MANE Select NP_003968.3:n.-109A=
NM_001302960.2:c.-109A= NP_001289889.1:n.-109A=