Canonical Allele Identifier: CA475509754

Gene: AIP

Linked Data

• ClinVar Variation Id: 1768205
• ClinVar RCV Id: RCV002387197
• MyVariant Identifiers: chr11:g.67258449G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490978G>A , CM000673.2:g.67490978G>A	GRCh38
NC_000011.9:g.67258449G>A , CM000673.1:g.67258449G>A	GRCh37
NC_000011.8:g.67015025G>A	NCBI36
NG_008969.1:g.12945G>A , LRG_460:g.12945G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1285G>A
ENST00000528641.7:c.789G>A	ENSP00000434982.3:p.Gly263=
ENST00000529797.2:n.1820G>A
ENST00000682324.1:c.469-19G>A	ENSP00000508017.1:n.469-19G>A
ENST00000682659.1:c.609G>A	ENSP00000507351.1:p.Gly203=
ENST00000683237.1:c.*118G>A	ENSP00000507343.1:n.*118G>A
ENST00000683856.1:c.801G>A	ENSP00000507979.1:p.Gly267=
ENST00000684006.1:c.*118G>A	ENSP00000507269.1:n.*118G>A
ENST00000684657.1:c.798G>A	ENSP00000507961.1:p.Gly266=
ENST00000279146.8:c.978G>A MANE Select	ENSP00000279146.3:p.Gly326=
ENST00000279146.7:c.978G>A	ENSP00000279146.3:p.Gly326=
NM_001302959.1:c.801G>A	NP_001289888.1:p.Gly267=
NM_001302960.1:c.*118G>A	NP_001289889.1:n.*118G>A
NM_003977.3:c.978G>A	NP_003968.3:p.Gly326=
XM_024448761.1:c.978G>A	XP_024304529.1:p.Gly326=
NM_003977.4:c.978G>A MANE Select	NP_003968.3:p.Gly326=
NM_001302960.2:c.*118G>A	NP_001289889.1:n.*118G>A
NM_001302959.2:c.801G>A	NP_001289888.1:p.Gly267=