Canonical Allele Identifier: CA6140983

Gene: AIP

Linked Data

• dbSNP Id: rs779831121
• ExAC: 11:67258286 G / A
• gnomAD v2: 11-67258286-G-A
• MyVariant Identifiers: chr11:g.67258286G>A (hg19) ; chr11:g.67490815G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490815G>A , CM000673.2:g.67490815G>A	GRCh38
NC_000011.9:g.67258286G>A , CM000673.1:g.67258286G>A	GRCh37
NC_000011.8:g.67014862G>A	NCBI36
NG_008969.1:g.12782G>A , LRG_460:g.12782G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1122G>A
ENST00000528641.7:c.626G>A	ENSP00000434982.3:p.Gly209Asp
ENST00000529797.2:n.1657G>A
ENST00000682324.1:c.469-182G>A	ENSP00000508017.1:n.469-182G>A
ENST00000682659.1:c.446G>A	ENSP00000507351.1:p.Gly149Asp
ENST00000682699.1:c.815G>A	ENSP00000507935.1:p.Gly272Asp
ENST00000683237.1:c.807G>A	ENSP00000507343.1:p.Gly269=
ENST00000683856.1:c.638G>A	ENSP00000507979.1:p.Gly213Asp
ENST00000684006.1:c.804G>A	ENSP00000507269.1:p.Gly268=
ENST00000684657.1:c.635G>A	ENSP00000507961.1:p.Gly212Asp
ENST00000279146.8:c.815G>A MANE Select	ENSP00000279146.3:p.Gly272Asp
ENST00000279146.7:c.815G>A	ENSP00000279146.3:p.Gly272Asp
ENST00000528641.6:c.626G>A	ENSP00000434982.2:p.Gly209Asp
NM_001302959.1:c.638G>A	NP_001289888.1:p.Gly213Asp
NM_001302960.1:c.807G>A	NP_001289889.1:p.Gly269=
NM_003977.3:c.815G>A	NP_003968.3:p.Gly272Asp
XM_024448761.1:c.815G>A	XP_024304529.1:p.Gly272Asp
NM_003977.4:c.815G>A MANE Select	NP_003968.3:p.Gly272Asp
NM_001302960.2:c.807G>A	NP_001289889.1:p.Gly269=
NM_001302959.2:c.638G>A	NP_001289888.1:p.Gly213Asp