Canonical Allele Identifier: CA1980172806
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491107G= , CM000673.2:g.67491107G= GRCh38
NC_000011.9:g.67258578G= , CM000673.1:g.67258578G= GRCh37
NC_000011.8:g.67015154G= NCBI36
NG_008969.1:g.13074G= , LRG_460:g.13074G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*114G= ENSP00000507961.1:n.*114G=
NM_001302959.1:c.*114G= NP_001289888.1:n.*114G=
NM_001302960.1:c.*247G= NP_001289889.1:n.*247G=
NM_003977.3:c.*114G= NP_003968.3:n.*114G=