Canonical Allele Identifier: CA381551127
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490173T>C , CM000673.2:g.67490173T>C GRCh38
NC_000011.9:g.67257644T>C , CM000673.1:g.67257644T>C GRCh37
NC_000011.8:g.67014220T>C NCBI36
NG_008969.1:g.12140T>C , LRG_460:g.12140T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.581T>C
ENST00000528641.7:c.415T>C ENSP00000434982.3:p.Tyr139His
ENST00000529797.2:n.1116T>C
ENST00000682324.1:c.468+718T>C ENSP00000508017.1:n.468+718T>C
ENST00000682659.1:c.235T>C ENSP00000507351.1:p.Tyr79His
ENST00000682699.1:c.604T>C ENSP00000507935.1:p.Tyr202His
ENST00000683237.1:c.604T>C ENSP00000507343.1:p.Tyr202His
ENST00000683856.1:c.427T>C ENSP00000507979.1:p.Tyr143His
ENST00000684006.1:c.604T>C ENSP00000507269.1:p.Tyr202His
ENST00000684657.1:c.424T>C ENSP00000507961.1:p.Tyr142His
ENST00000279146.8:c.604T>C MANE Select ENSP00000279146.3:p.Tyr202His
ENST00000279146.7:c.604T>C ENSP00000279146.3:p.Tyr202His
ENST00000525341.1:c.256T>C ENSP00000476993.1:p.Tyr86His
ENST00000528641.6:c.415T>C ENSP00000434982.2:p.Tyr139His
NM_001302959.1:c.427T>C NP_001289888.1:p.Tyr143His
NM_001302960.1:c.604T>C NP_001289889.1:p.Tyr202His
NM_003977.3:c.604T>C NP_003968.3:p.Tyr202His
XM_024448761.1:c.604T>C XP_024304529.1:p.Tyr202His
NM_003977.4:c.604T>C MANE Select NP_003968.3:p.Tyr202His
NM_001302960.2:c.604T>C NP_001289889.1:p.Tyr202His
NM_001302959.2:c.427T>C NP_001289888.1:p.Tyr143His