Canonical Allele Identifier: CA381554874

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258325A>G (hg19) ; chr11:g.67490854A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490854A>G , CM000673.2:g.67490854A>G	GRCh38
NC_000011.9:g.67258325A>G , CM000673.1:g.67258325A>G	GRCh37
NC_000011.8:g.67014901A>G	NCBI36
NG_008969.1:g.12821A>G , LRG_460:g.12821A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1161A>G
ENST00000528641.7:c.665A>G	ENSP00000434982.3:p.Gln222Arg
ENST00000529797.2:n.1696A>G
ENST00000682324.1:c.469-143A>G	ENSP00000508017.1:n.469-143A>G
ENST00000682659.1:c.485A>G	ENSP00000507351.1:p.Gln162Arg
ENST00000682699.1:c.854A>G	ENSP00000507935.1:p.Gln285Arg
ENST00000683237.1:c.846A>G	ENSP00000507343.1:p.Pro282=
ENST00000683856.1:c.677A>G	ENSP00000507979.1:p.Gln226Arg
ENST00000684006.1:c.843A>G	ENSP00000507269.1:p.Pro281=
ENST00000684657.1:c.674A>G	ENSP00000507961.1:p.Gln225Arg
ENST00000279146.8:c.854A>G MANE Select	ENSP00000279146.3:p.Gln285Arg
ENST00000279146.7:c.854A>G	ENSP00000279146.3:p.Gln285Arg
ENST00000528641.6:c.665A>G	ENSP00000434982.2:p.Gln222Arg
NM_001302959.1:c.677A>G	NP_001289888.1:p.Gln226Arg
NM_001302960.1:c.846A>G	NP_001289889.1:p.Pro282=
NM_003977.3:c.854A>G	NP_003968.3:p.Gln285Arg
XM_024448761.1:c.854A>G	XP_024304529.1:p.Gln285Arg
NM_003977.4:c.854A>G MANE Select	NP_003968.3:p.Gln285Arg
NM_001302960.2:c.846A>G	NP_001289889.1:p.Pro282=
NM_001302959.2:c.677A>G	NP_001289888.1:p.Gln226Arg