Canonical Allele Identifier: CA475392551

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67256827T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489356T>A , CM000673.2:g.67489356T>A	GRCh38
NC_000011.9:g.67256827T>A , CM000673.1:g.67256827T>A	GRCh37
NC_000011.8:g.67013403T>A	NCBI36
NG_008969.1:g.11323T>A , LRG_460:g.11323T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.346T>A
ENST00000528641.7:c.280-682T>A	ENSP00000434982.3:n.280-682T>A
ENST00000529797.2:n.299T>A
ENST00000682324.1:c.369T>A	ENSP00000508017.1:p.Gly123=
ENST00000682659.1:c.100-682T>A	ENSP00000507351.1:n.100-682T>A
ENST00000682699.1:c.369T>A	ENSP00000507935.1:p.Gly123=
ENST00000683237.1:c.369T>A	ENSP00000507343.1:p.Gly123=
ENST00000683856.1:c.192T>A	ENSP00000507979.1:p.Gly64=
ENST00000684006.1:c.369T>A	ENSP00000507269.1:p.Gly123=
ENST00000684657.1:c.189T>A	ENSP00000507961.1:p.Gly63=
ENST00000279146.8:c.369T>A MANE Select	ENSP00000279146.3:p.Gly123=
ENST00000279146.7:c.369T>A	ENSP00000279146.3:p.Gly123=
ENST00000525341.1:c.21T>A	ENSP00000476993.1:p.Gly7=
ENST00000528641.6:c.280-682T>A	ENSP00000434982.2:n.280-682T>A
ENST00000529797.1:n.479T>A
NM_001302959.1:c.192T>A	NP_001289888.1:p.Gly64=
NM_001302960.1:c.369T>A	NP_001289889.1:p.Gly123=
NM_003977.3:c.369T>A	NP_003968.3:p.Gly123=
XM_024448761.1:c.369T>A	XP_024304529.1:p.Gly123=
NM_003977.4:c.369T>A MANE Select	NP_003968.3:p.Gly123=
NM_001302960.2:c.369T>A	NP_001289889.1:p.Gly123=
NM_001302959.2:c.192T>A	NP_001289888.1:p.Gly64=