Canonical Allele Identifier: CA475509212

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257828G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490357G>A , CM000673.2:g.67490357G>A	GRCh38
NC_000011.9:g.67257828G>A , CM000673.1:g.67257828G>A	GRCh37
NC_000011.8:g.67014404G>A	NCBI36
NG_008969.1:g.12324G>A , LRG_460:g.12324G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.664G>A
ENST00000528641.7:c.498G>A	ENSP00000434982.3:p.Gln166=
ENST00000529797.2:n.1199G>A
ENST00000682324.1:c.469-640G>A	ENSP00000508017.1:n.469-640G>A
ENST00000682659.1:c.318G>A	ENSP00000507351.1:p.Gln106=
ENST00000682699.1:c.687G>A	ENSP00000507935.1:p.Gln229=
ENST00000683237.1:c.687G>A	ENSP00000507343.1:p.Gln229=
ENST00000683856.1:c.510G>A	ENSP00000507979.1:p.Gln170=
ENST00000684006.1:c.687G>A	ENSP00000507269.1:p.Gln229=
ENST00000684657.1:c.507G>A	ENSP00000507961.1:p.Gln169=
ENST00000279146.8:c.687G>A MANE Select	ENSP00000279146.3:p.Gln229=
ENST00000279146.7:c.687G>A	ENSP00000279146.3:p.Gln229=
ENST00000525341.1:c.339G>A	ENSP00000476993.1:p.Gln113=
ENST00000528641.6:c.498G>A	ENSP00000434982.2:p.Gln166=
NM_001302959.1:c.510G>A	NP_001289888.1:p.Gln170=
NM_001302960.1:c.687G>A	NP_001289889.1:p.Gln229=
NM_003977.3:c.687G>A	NP_003968.3:p.Gln229=
XM_024448761.1:c.687G>A	XP_024304529.1:p.Gln229=
NM_003977.4:c.687G>A MANE Select	NP_003968.3:p.Gln229=
NM_001302960.2:c.687G>A	NP_001289889.1:p.Gln229=
NM_001302959.2:c.510G>A	NP_001289888.1:p.Gln170=