Canonical Allele Identifier: CA381551249
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490193C>G , CM000673.2:g.67490193C>G GRCh38
NC_000011.9:g.67257664C>G , CM000673.1:g.67257664C>G GRCh37
NC_000011.8:g.67014240C>G NCBI36
NG_008969.1:g.12160C>G , LRG_460:g.12160C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.601C>G
ENST00000528641.7:c.435C>G ENSP00000434982.3:p.Cys145Trp
ENST00000529797.2:n.1136C>G
ENST00000682324.1:c.468+738C>G ENSP00000508017.1:n.468+738C>G
ENST00000682659.1:c.255C>G ENSP00000507351.1:p.Cys85Trp
ENST00000682699.1:c.624C>G ENSP00000507935.1:p.Cys208Trp
ENST00000683237.1:c.624C>G ENSP00000507343.1:p.Cys208Trp
ENST00000683856.1:c.447C>G ENSP00000507979.1:p.Cys149Trp
ENST00000684006.1:c.624C>G ENSP00000507269.1:p.Cys208Trp
ENST00000684657.1:c.444C>G ENSP00000507961.1:p.Cys148Trp
ENST00000279146.8:c.624C>G MANE Select ENSP00000279146.3:p.Cys208Trp
ENST00000279146.7:c.624C>G ENSP00000279146.3:p.Cys208Trp
ENST00000525341.1:c.276C>G ENSP00000476993.1:p.Cys92Trp
ENST00000528641.6:c.435C>G ENSP00000434982.2:p.Cys145Trp
NM_001302959.1:c.447C>G NP_001289888.1:p.Cys149Trp
NM_001302960.1:c.624C>G NP_001289889.1:p.Cys208Trp
NM_003977.3:c.624C>G NP_003968.3:p.Cys208Trp
XM_024448761.1:c.624C>G XP_024304529.1:p.Cys208Trp
NM_003977.4:c.624C>G MANE Select NP_003968.3:p.Cys208Trp
NM_001302960.2:c.624C>G NP_001289889.1:p.Cys208Trp
NM_001302959.2:c.447C>G NP_001289888.1:p.Cys149Trp