Canonical Allele Identifier: CA2614618073
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67483043-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483043C>A , CM000673.2:g.67483043C>A GRCh38
NC_000011.9:g.67250514C>A , CM000673.1:g.67250514C>A GRCh37
NC_000011.8:g.67007090C>A NCBI36
NG_008969.1:g.5010C>A , LRG_460:g.5010C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000528641.7:c.-116C>A ENSP00000434982.3:n.-116C>A
ENST00000682699.1:c.-116C>A ENSP00000507935.1:n.-116C>A
ENST00000279146.8:c.-116C>A MANE Select ENSP00000279146.3:n.-116C>A
ENST00000279146.7:c.-116C>A ENSP00000279146.3:n.-116C>A
ENST00000528641.6:c.-116C>A ENSP00000434982.2:n.-116C>A
NM_001302960.1:c.-116C>A NP_001289889.1:n.-116C>A
NM_003977.3:c.-116C>A NP_003968.3:n.-116C>A
XM_024448761.1:c.-116C>A XP_024304529.1:n.-116C>A
NM_003977.4:c.-116C>A MANE Select NP_003968.3:n.-116C>A
NM_001302960.2:c.-116C>A NP_001289889.1:n.-116C>A
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