Canonical Allele Identifier: CA475509525

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258323C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490852C>A , CM000673.2:g.67490852C>A	GRCh38
NC_000011.9:g.67258323C>A , CM000673.1:g.67258323C>A	GRCh37
NC_000011.8:g.67014899C>A	NCBI36
NG_008969.1:g.12819C>A , LRG_460:g.12819C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1159C>A
ENST00000528641.7:c.663C>A	ENSP00000434982.3:p.Ala221=
ENST00000529797.2:n.1694C>A
ENST00000682324.1:c.469-145C>A	ENSP00000508017.1:n.469-145C>A
ENST00000682659.1:c.483C>A	ENSP00000507351.1:p.Ala161=
ENST00000682699.1:c.852C>A	ENSP00000507935.1:p.Ala284=
ENST00000683237.1:c.844C>A	ENSP00000507343.1:p.Pro282Thr
ENST00000683856.1:c.675C>A	ENSP00000507979.1:p.Ala225=
ENST00000684006.1:c.841C>A	ENSP00000507269.1:p.Pro281Thr
ENST00000684657.1:c.672C>A	ENSP00000507961.1:p.Ala224=
ENST00000279146.8:c.852C>A MANE Select	ENSP00000279146.3:p.Ala284=
ENST00000279146.7:c.852C>A	ENSP00000279146.3:p.Ala284=
ENST00000528641.6:c.663C>A	ENSP00000434982.2:p.Ala221=
NM_001302959.1:c.675C>A	NP_001289888.1:p.Ala225=
NM_001302960.1:c.844C>A	NP_001289889.1:p.Pro282Thr
NM_003977.3:c.852C>A	NP_003968.3:p.Ala284=
XM_024448761.1:c.852C>A	XP_024304529.1:p.Ala284=
NM_003977.4:c.852C>A MANE Select	NP_003968.3:p.Ala284=
NM_001302960.2:c.844C>A	NP_001289889.1:p.Pro282Thr
NM_001302959.2:c.675C>A	NP_001289888.1:p.Ala225=