Canonical Allele Identifier: CA475509176

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257789A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490318A>G , CM000673.2:g.67490318A>G	GRCh38
NC_000011.9:g.67257789A>G , CM000673.1:g.67257789A>G	GRCh37
NC_000011.8:g.67014365A>G	NCBI36
NG_008969.1:g.12285A>G , LRG_460:g.12285A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.625A>G
ENST00000528641.7:c.459A>G	ENSP00000434982.3:p.Glu153=
ENST00000529797.2:n.1160A>G
ENST00000682324.1:c.469-679A>G	ENSP00000508017.1:n.469-679A>G
ENST00000682659.1:c.279A>G	ENSP00000507351.1:p.Glu93=
ENST00000682699.1:c.648A>G	ENSP00000507935.1:p.Glu216=
ENST00000683237.1:c.648A>G	ENSP00000507343.1:p.Glu216=
ENST00000683856.1:c.471A>G	ENSP00000507979.1:p.Glu157=
ENST00000684006.1:c.648A>G	ENSP00000507269.1:p.Glu216=
ENST00000684657.1:c.468A>G	ENSP00000507961.1:p.Glu156=
ENST00000279146.8:c.648A>G MANE Select	ENSP00000279146.3:p.Glu216=
ENST00000279146.7:c.648A>G	ENSP00000279146.3:p.Glu216=
ENST00000525341.1:c.300A>G	ENSP00000476993.1:p.Glu100=
ENST00000528641.6:c.459A>G	ENSP00000434982.2:p.Glu153=
NM_001302959.1:c.471A>G	NP_001289888.1:p.Glu157=
NM_001302960.1:c.648A>G	NP_001289889.1:p.Glu216=
NM_003977.3:c.648A>G	NP_003968.3:p.Glu216=
XM_024448761.1:c.648A>G	XP_024304529.1:p.Glu216=
NM_003977.4:c.648A>G MANE Select	NP_003968.3:p.Glu216=
NM_001302960.2:c.648A>G	NP_001289889.1:p.Glu216=
NM_001302959.2:c.471A>G	NP_001289888.1:p.Glu157=