Canonical Allele Identifier: CA381551088

Gene: AIP

Linked Data

• gnomAD v4: 11-67490167-G-A
• MyVariant Identifiers: chr11:g.67257638G>A (hg19) ; chr11:g.67490167G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490167G>A , CM000673.2:g.67490167G>A	GRCh38
NC_000011.9:g.67257638G>A , CM000673.1:g.67257638G>A	GRCh37
NC_000011.8:g.67014214G>A	NCBI36
NG_008969.1:g.12134G>A , LRG_460:g.12134G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.575G>A
ENST00000528641.7:c.409G>A	ENSP00000434982.3:p.Ala137Thr
ENST00000529797.2:n.1110G>A
ENST00000682324.1:c.468+712G>A	ENSP00000508017.1:n.468+712G>A
ENST00000682659.1:c.229G>A	ENSP00000507351.1:p.Ala77Thr
ENST00000682699.1:c.598G>A	ENSP00000507935.1:p.Ala200Thr
ENST00000683237.1:c.598G>A	ENSP00000507343.1:p.Ala200Thr
ENST00000683856.1:c.421G>A	ENSP00000507979.1:p.Ala141Thr
ENST00000684006.1:c.598G>A	ENSP00000507269.1:p.Ala200Thr
ENST00000684657.1:c.418G>A	ENSP00000507961.1:p.Ala140Thr
ENST00000279146.8:c.598G>A MANE Select	ENSP00000279146.3:p.Ala200Thr
ENST00000279146.7:c.598G>A	ENSP00000279146.3:p.Ala200Thr
ENST00000525341.1:c.250G>A	ENSP00000476993.1:p.Ala84Thr
ENST00000528641.6:c.409G>A	ENSP00000434982.2:p.Ala137Thr
NM_001302959.1:c.421G>A	NP_001289888.1:p.Ala141Thr
NM_001302960.1:c.598G>A	NP_001289889.1:p.Ala200Thr
NM_003977.3:c.598G>A	NP_003968.3:p.Ala200Thr
XM_024448761.1:c.598G>A	XP_024304529.1:p.Ala200Thr
NM_003977.4:c.598G>A MANE Select	NP_003968.3:p.Ala200Thr
NM_001302960.2:c.598G>A	NP_001289889.1:p.Ala200Thr
NM_001302959.2:c.421G>A	NP_001289888.1:p.Ala141Thr