Canonical Allele Identifier: CA381555288

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258376T>A (hg19) ; chr11:g.67490905T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490905T>A , CM000673.2:g.67490905T>A	GRCh38
NC_000011.9:g.67258376T>A , CM000673.1:g.67258376T>A	GRCh37
NC_000011.8:g.67014952T>A	NCBI36
NG_008969.1:g.12872T>A , LRG_460:g.12872T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1212T>A
ENST00000528641.7:c.716T>A	ENSP00000434982.3:p.Val239Glu
ENST00000529797.2:n.1747T>A
ENST00000682324.1:c.469-92T>A	ENSP00000508017.1:n.469-92T>A
ENST00000682659.1:c.536T>A	ENSP00000507351.1:p.Val179Glu
ENST00000682699.1:c.905T>A	ENSP00000507935.1:p.Val302Glu
ENST00000683237.1:c.*45T>A	ENSP00000507343.1:n.*45T>A
ENST00000683856.1:c.728T>A	ENSP00000507979.1:p.Val243Glu
ENST00000684006.1:c.*45T>A	ENSP00000507269.1:n.*45T>A
ENST00000684657.1:c.725T>A	ENSP00000507961.1:p.Val242Glu
ENST00000279146.8:c.905T>A MANE Select	ENSP00000279146.3:p.Val302Glu
ENST00000279146.7:c.905T>A	ENSP00000279146.3:p.Val302Glu
NM_001302959.1:c.728T>A	NP_001289888.1:p.Val243Glu
NM_001302960.1:c.*45T>A	NP_001289889.1:n.*45T>A
NM_003977.3:c.905T>A	NP_003968.3:p.Val302Glu
XM_024448761.1:c.905T>A	XP_024304529.1:p.Val302Glu
NM_003977.4:c.905T>A MANE Select	NP_003968.3:p.Val302Glu
NM_001302960.2:c.*45T>A	NP_001289889.1:n.*45T>A
NM_001302959.2:c.728T>A	NP_001289888.1:p.Val243Glu