Canonical Allele Identifier: CA381554763

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258315C>G (hg19) ; chr11:g.67490844C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490844C>G , CM000673.2:g.67490844C>G	GRCh38
NC_000011.9:g.67258315C>G , CM000673.1:g.67258315C>G	GRCh37
NC_000011.8:g.67014891C>G	NCBI36
NG_008969.1:g.12811C>G , LRG_460:g.12811C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1151C>G
ENST00000528641.7:c.655C>G	ENSP00000434982.3:p.Gln219Glu
ENST00000529797.2:n.1686C>G
ENST00000682324.1:c.469-153C>G	ENSP00000508017.1:n.469-153C>G
ENST00000682659.1:c.475C>G	ENSP00000507351.1:p.Gln159Glu
ENST00000682699.1:c.844C>G	ENSP00000507935.1:p.Gln282Glu
ENST00000683237.1:c.836C>G	ENSP00000507343.1:p.Pro279Arg
ENST00000683856.1:c.667C>G	ENSP00000507979.1:p.Gln223Glu
ENST00000684006.1:c.833C>G	ENSP00000507269.1:p.Pro278Arg
ENST00000684657.1:c.664C>G	ENSP00000507961.1:p.Gln222Glu
ENST00000279146.8:c.844C>G MANE Select	ENSP00000279146.3:p.Gln282Glu
ENST00000279146.7:c.844C>G	ENSP00000279146.3:p.Gln282Glu
ENST00000528641.6:c.655C>G	ENSP00000434982.2:p.Gln219Glu
NM_001302959.1:c.667C>G	NP_001289888.1:p.Gln223Glu
NM_001302960.1:c.836C>G	NP_001289889.1:p.Pro279Arg
NM_003977.3:c.844C>G	NP_003968.3:p.Gln282Glu
XM_024448761.1:c.844C>G	XP_024304529.1:p.Gln282Glu
NM_003977.4:c.844C>G MANE Select	NP_003968.3:p.Gln282Glu
NM_001302960.2:c.836C>G	NP_001289889.1:p.Pro279Arg
NM_001302959.2:c.667C>G	NP_001289888.1:p.Gln223Glu