Canonical Allele Identifier: CA381554319

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258265T>G (hg19) ; chr11:g.67490794T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490794T>G , CM000673.2:g.67490794T>G	GRCh38
NC_000011.9:g.67258265T>G , CM000673.1:g.67258265T>G	GRCh37
NC_000011.8:g.67014841T>G	NCBI36
NG_008969.1:g.12761T>G , LRG_460:g.12761T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1101T>G
ENST00000528641.7:c.605T>G	ENSP00000434982.3:p.Val202Gly
ENST00000529797.2:n.1636T>G
ENST00000682324.1:c.469-203T>G	ENSP00000508017.1:n.469-203T>G
ENST00000682659.1:c.425T>G	ENSP00000507351.1:p.Val142Gly
ENST00000682699.1:c.794T>G	ENSP00000507935.1:p.Val265Gly
ENST00000683237.1:c.786T>G	ENSP00000507343.1:p.Arg262=
ENST00000683856.1:c.617T>G	ENSP00000507979.1:p.Val206Gly
ENST00000684006.1:c.788-5T>G	ENSP00000507269.1:n.788-5T>G
ENST00000684657.1:c.614T>G	ENSP00000507961.1:p.Val205Gly
ENST00000279146.8:c.794T>G MANE Select	ENSP00000279146.3:p.Val265Gly
ENST00000279146.7:c.794T>G	ENSP00000279146.3:p.Val265Gly
ENST00000528641.6:c.605T>G	ENSP00000434982.2:p.Val202Gly
NM_001302959.1:c.617T>G	NP_001289888.1:p.Val206Gly
NM_001302960.1:c.786T>G	NP_001289889.1:p.Arg262=
NM_003977.3:c.794T>G	NP_003968.3:p.Val265Gly
XM_024448761.1:c.794T>G	XP_024304529.1:p.Val265Gly
NM_003977.4:c.794T>G MANE Select	NP_003968.3:p.Val265Gly
NM_001302960.2:c.786T>G	NP_001289889.1:p.Arg262=
NM_001302959.2:c.617T>G	NP_001289888.1:p.Val206Gly