Canonical Allele Identifier: CA475509741

Gene: AIP

Linked Data

• gnomAD v4: 11-67490967-C-A
• MyVariant Identifiers: chr11:g.67258438C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490967C>A , CM000673.2:g.67490967C>A	GRCh38
NC_000011.9:g.67258438C>A , CM000673.1:g.67258438C>A	GRCh37
NC_000011.8:g.67015014C>A	NCBI36
NG_008969.1:g.12934C>A , LRG_460:g.12934C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1274C>A
ENST00000528641.7:c.778C>A	ENSP00000434982.3:p.Arg260=
ENST00000529797.2:n.1809C>A
ENST00000682324.1:c.469-30C>A	ENSP00000508017.1:n.469-30C>A
ENST00000682659.1:c.598C>A	ENSP00000507351.1:p.Arg200=
ENST00000683237.1:c.*107C>A	ENSP00000507343.1:n.*107C>A
ENST00000683856.1:c.790C>A	ENSP00000507979.1:p.Arg264=
ENST00000684006.1:c.*107C>A	ENSP00000507269.1:n.*107C>A
ENST00000684657.1:c.787C>A	ENSP00000507961.1:p.Arg263=
ENST00000279146.8:c.967C>A MANE Select	ENSP00000279146.3:p.Arg323=
ENST00000279146.7:c.967C>A	ENSP00000279146.3:p.Arg323=
NM_001302959.1:c.790C>A	NP_001289888.1:p.Arg264=
NM_001302960.1:c.*107C>A	NP_001289889.1:n.*107C>A
NM_003977.3:c.967C>A	NP_003968.3:p.Arg323=
XM_024448761.1:c.967C>A	XP_024304529.1:p.Arg323=
NM_003977.4:c.967C>A MANE Select	NP_003968.3:p.Arg323=
NM_001302960.2:c.*107C>A	NP_001289889.1:n.*107C>A
NM_001302959.2:c.790C>A	NP_001289888.1:p.Arg264=