Canonical Allele Identifier: CA381549222

Gene: AIP

Linked Data

• ClinVar Variation Id: 1717805
• ClinVar RCV Id: RCV002297814
• gnomAD v4: 11-67489337-G-A
• MyVariant Identifiers: chr11:g.67256808G>A (hg19) ; chr11:g.67489337G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489337G>A , CM000673.2:g.67489337G>A	GRCh38
NC_000011.9:g.67256808G>A , CM000673.1:g.67256808G>A	GRCh37
NC_000011.8:g.67013384G>A	NCBI36
NG_008969.1:g.11304G>A , LRG_460:g.11304G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.327G>A
ENST00000528641.7:c.280-701G>A	ENSP00000434982.3:n.280-701G>A
ENST00000529797.2:n.280G>A
ENST00000682324.1:c.350G>A	ENSP00000508017.1:p.Gly117Asp
ENST00000682659.1:c.100-701G>A	ENSP00000507351.1:n.100-701G>A
ENST00000682699.1:c.350G>A	ENSP00000507935.1:p.Gly117Asp
ENST00000683237.1:c.350G>A	ENSP00000507343.1:p.Gly117Asp
ENST00000683856.1:c.173G>A	ENSP00000507979.1:p.Gly58Asp
ENST00000684006.1:c.350G>A	ENSP00000507269.1:p.Gly117Asp
ENST00000684657.1:c.170G>A	ENSP00000507961.1:p.Gly57Asp
ENST00000279146.8:c.350G>A MANE Select	ENSP00000279146.3:p.Gly117Asp
ENST00000279146.7:c.350G>A	ENSP00000279146.3:p.Gly117Asp
ENST00000525341.1:c.2G>A	ENSP00000476993.1:p.Gly1Asp
ENST00000528641.6:c.280-701G>A	ENSP00000434982.2:n.280-701G>A
ENST00000529797.1:n.460G>A
NM_001302959.1:c.173G>A	NP_001289888.1:p.Gly58Asp
NM_001302960.1:c.350G>A	NP_001289889.1:p.Gly117Asp
NM_003977.3:c.350G>A	NP_003968.3:p.Gly117Asp
XM_024448761.1:c.350G>A	XP_024304529.1:p.Gly117Asp
NM_003977.4:c.350G>A MANE Select	NP_003968.3:p.Gly117Asp
NM_001302960.2:c.350G>A	NP_001289889.1:p.Gly117Asp
NM_001302959.2:c.173G>A	NP_001289888.1:p.Gly58Asp