Canonical Allele Identifier: CA224165894

Gene: AIP

Linked Data

• dbSNP Id: rs909828555
• MyVariant Identifiers: chr11:g.67258304T>G (hg19) ; chr11:g.67490833T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490833T>G , CM000673.2:g.67490833T>G	GRCh38
NC_000011.9:g.67258304T>G , CM000673.1:g.67258304T>G	GRCh37
NC_000011.8:g.67014880T>G	NCBI36
NG_008969.1:g.12800T>G , LRG_460:g.12800T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1140T>G
ENST00000528641.7:c.644T>G	ENSP00000434982.3:p.Val215Gly
ENST00000529797.2:n.1675T>G
ENST00000682324.1:c.469-164T>G	ENSP00000508017.1:n.469-164T>G
ENST00000682659.1:c.464T>G	ENSP00000507351.1:p.Val155Gly
ENST00000682699.1:c.833T>G	ENSP00000507935.1:p.Val278Gly
ENST00000683237.1:c.825T>G	ENSP00000507343.1:p.Arg275=
ENST00000683856.1:c.656T>G	ENSP00000507979.1:p.Val219Gly
ENST00000684006.1:c.822T>G	ENSP00000507269.1:p.Arg274=
ENST00000684657.1:c.653T>G	ENSP00000507961.1:p.Val218Gly
ENST00000279146.8:c.833T>G MANE Select	ENSP00000279146.3:p.Val278Gly
ENST00000279146.7:c.833T>G	ENSP00000279146.3:p.Val278Gly
ENST00000528641.6:c.644T>G	ENSP00000434982.2:p.Val215Gly
NM_001302959.1:c.656T>G	NP_001289888.1:p.Val219Gly
NM_001302960.1:c.825T>G	NP_001289889.1:p.Arg275=
NM_003977.3:c.833T>G	NP_003968.3:p.Val278Gly
XM_024448761.1:c.833T>G	XP_024304529.1:p.Val278Gly
NM_003977.4:c.833T>G MANE Select	NP_003968.3:p.Val278Gly
NM_001302960.2:c.825T>G	NP_001289889.1:p.Arg275=
NM_001302959.2:c.656T>G	NP_001289888.1:p.Val219Gly