Canonical Allele Identifier: CA1980172321
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490150A= , CM000673.2:g.67490150A= GRCh38
NC_000011.9:g.67257621A= , CM000673.1:g.67257621A= GRCh37
NC_000011.8:g.67014197A= NCBI36
NG_008969.1:g.12117A= , LRG_460:g.12117A=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.558A=
ENST00000528641.7:c.392A= ENSP00000434982.3:p.His131=
ENST00000529797.2:n.1093A=
ENST00000682324.1:c.468+695A= ENSP00000508017.1:n.468+695A=
ENST00000682659.1:c.212A= ENSP00000507351.1:p.His71=
ENST00000682699.1:c.581A= ENSP00000507935.1:p.His194=
ENST00000683237.1:c.581A= ENSP00000507343.1:p.His194=
ENST00000683856.1:c.404A= ENSP00000507979.1:p.His135=
ENST00000684006.1:c.581A= ENSP00000507269.1:p.His194=
ENST00000684657.1:c.401A= ENSP00000507961.1:p.His134=
ENST00000279146.8:c.581A= MANE Select ENSP00000279146.3:p.His194=
ENST00000279146.7:c.581A= ENSP00000279146.3:p.His194=
ENST00000525341.1:c.233A= ENSP00000476993.1:p.His78=
ENST00000528641.6:c.392A= ENSP00000434982.2:p.His131=
NM_001302959.1:c.404A= NP_001289888.1:p.His135=
NM_001302960.1:c.581A= NP_001289889.1:p.His194=
NM_003977.3:c.581A= NP_003968.3:p.His194=
XM_024448761.1:c.581A= XP_024304529.1:p.His194=
NM_003977.4:c.581A= MANE Select NP_003968.3:p.His194=
NM_001302960.2:c.581A= NP_001289889.1:p.His194=
NM_001302959.2:c.404A= NP_001289888.1:p.His135=