Canonical Allele Identifier: CA2614618103
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483061A>T , CM000673.2:g.67483061A>T GRCh38
NC_000011.9:g.67250532A>T , CM000673.1:g.67250532A>T GRCh37
NC_000011.8:g.67007108A>T NCBI36
NG_008969.1:g.5028A>T , LRG_460:g.5028A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000528641.7:c.-98A>T ENSP00000434982.3:n.-98A>T
ENST00000682699.1:c.-98A>T ENSP00000507935.1:n.-98A>T
ENST00000279146.8:c.-98A>T MANE Select ENSP00000279146.3:n.-98A>T
ENST00000279146.7:c.-98A>T ENSP00000279146.3:n.-98A>T
ENST00000528641.6:c.-98A>T ENSP00000434982.2:n.-98A>T
ENST00000529797.1:n.13A>T
NM_001302960.1:c.-98A>T NP_001289889.1:n.-98A>T
NM_003977.3:c.-98A>T NP_003968.3:n.-98A>T
XM_024448761.1:c.-98A>T XP_024304529.1:n.-98A>T
NM_003977.4:c.-98A>T MANE Select NP_003968.3:n.-98A>T
NM_001302960.2:c.-98A>T NP_001289889.1:n.-98A>T