Canonical Allele Identifier: CA475509173

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257586C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490115C>A , CM000673.2:g.67490115C>A	GRCh38
NC_000011.9:g.67257586C>A , CM000673.1:g.67257586C>A	GRCh37
NC_000011.8:g.67014162C>A	NCBI36
NG_008969.1:g.12082C>A , LRG_460:g.12082C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.523C>A
ENST00000528641.7:c.357C>A	ENSP00000434982.3:p.Ile119=
ENST00000529797.2:n.1058C>A
ENST00000682324.1:c.468+660C>A	ENSP00000508017.1:n.468+660C>A
ENST00000682659.1:c.177C>A	ENSP00000507351.1:p.Ile59=
ENST00000682699.1:c.546C>A	ENSP00000507935.1:p.Ile182=
ENST00000683237.1:c.546C>A	ENSP00000507343.1:p.Ile182=
ENST00000683856.1:c.369C>A	ENSP00000507979.1:p.Ile123=
ENST00000684006.1:c.546C>A	ENSP00000507269.1:p.Ile182=
ENST00000684657.1:c.366C>A	ENSP00000507961.1:p.Ile122=
ENST00000279146.8:c.546C>A MANE Select	ENSP00000279146.3:p.Ile182=
ENST00000279146.7:c.546C>A	ENSP00000279146.3:p.Ile182=
ENST00000525341.1:c.198C>A	ENSP00000476993.1:p.Ile66=
ENST00000528641.6:c.357C>A	ENSP00000434982.2:p.Ile119=
NM_001302959.1:c.369C>A	NP_001289888.1:p.Ile123=
NM_001302960.1:c.546C>A	NP_001289889.1:p.Ile182=
NM_003977.3:c.546C>A	NP_003968.3:p.Ile182=
XM_024448761.1:c.546C>A	XP_024304529.1:p.Ile182=
NM_003977.4:c.546C>A MANE Select	NP_003968.3:p.Ile182=
NM_001302960.2:c.546C>A	NP_001289889.1:p.Ile182=
NM_001302959.2:c.369C>A	NP_001289888.1:p.Ile123=