Canonical Allele Identifier: CA475392559

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67256833A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489362A>T , CM000673.2:g.67489362A>T	GRCh38
NC_000011.9:g.67256833A>T , CM000673.1:g.67256833A>T	GRCh37
NC_000011.8:g.67013409A>T	NCBI36
NG_008969.1:g.11329A>T , LRG_460:g.11329A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.352A>T
ENST00000528641.7:c.280-676A>T	ENSP00000434982.3:n.280-676A>T
ENST00000529797.2:n.305A>T
ENST00000682324.1:c.375A>T	ENSP00000508017.1:p.Ala125=
ENST00000682659.1:c.100-676A>T	ENSP00000507351.1:n.100-676A>T
ENST00000682699.1:c.375A>T	ENSP00000507935.1:p.Ala125=
ENST00000683237.1:c.375A>T	ENSP00000507343.1:p.Ala125=
ENST00000683856.1:c.198A>T	ENSP00000507979.1:p.Ala66=
ENST00000684006.1:c.375A>T	ENSP00000507269.1:p.Ala125=
ENST00000684657.1:c.195A>T	ENSP00000507961.1:p.Ala65=
ENST00000279146.8:c.375A>T MANE Select	ENSP00000279146.3:p.Ala125=
ENST00000279146.7:c.375A>T	ENSP00000279146.3:p.Ala125=
ENST00000525341.1:c.27A>T	ENSP00000476993.1:p.Ala9=
ENST00000528641.6:c.280-676A>T	ENSP00000434982.2:n.280-676A>T
ENST00000529797.1:n.485A>T
NM_001302959.1:c.198A>T	NP_001289888.1:p.Ala66=
NM_001302960.1:c.375A>T	NP_001289889.1:p.Ala125=
NM_003977.3:c.375A>T	NP_003968.3:p.Ala125=
XM_024448761.1:c.375A>T	XP_024304529.1:p.Ala125=
NM_003977.4:c.375A>T MANE Select	NP_003968.3:p.Ala125=
NM_001302960.2:c.375A>T	NP_001289889.1:p.Ala125=
NM_001302959.2:c.198A>T	NP_001289888.1:p.Ala66=