Canonical Allele Identifier: CA381551112

Gene: AIP

Linked Data

• ClinVar Variation Id: 1020160
• ClinVar RCV Id: RCV001319695
• dbSNP Id: rs1865874360
• MyVariant Identifiers: chr11:g.67257642A>G (hg19) ; chr11:g.67490171A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490171A>G , CM000673.2:g.67490171A>G	GRCh38
NC_000011.9:g.67257642A>G , CM000673.1:g.67257642A>G	GRCh37
NC_000011.8:g.67014218A>G	NCBI36
NG_008969.1:g.12138A>G , LRG_460:g.12138A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.579A>G
ENST00000528641.7:c.413A>G	ENSP00000434982.3:p.Lys138Arg
ENST00000529797.2:n.1114A>G
ENST00000682324.1:c.468+716A>G	ENSP00000508017.1:n.468+716A>G
ENST00000682659.1:c.233A>G	ENSP00000507351.1:p.Lys78Arg
ENST00000682699.1:c.602A>G	ENSP00000507935.1:p.Lys201Arg
ENST00000683237.1:c.602A>G	ENSP00000507343.1:p.Lys201Arg
ENST00000683856.1:c.425A>G	ENSP00000507979.1:p.Lys142Arg
ENST00000684006.1:c.602A>G	ENSP00000507269.1:p.Lys201Arg
ENST00000684657.1:c.422A>G	ENSP00000507961.1:p.Lys141Arg
ENST00000279146.8:c.602A>G MANE Select	ENSP00000279146.3:p.Lys201Arg
ENST00000279146.7:c.602A>G	ENSP00000279146.3:p.Lys201Arg
ENST00000525341.1:c.254A>G	ENSP00000476993.1:p.Lys85Arg
ENST00000528641.6:c.413A>G	ENSP00000434982.2:p.Lys138Arg
NM_001302959.1:c.425A>G	NP_001289888.1:p.Lys142Arg
NM_001302960.1:c.602A>G	NP_001289889.1:p.Lys201Arg
NM_003977.3:c.602A>G	NP_003968.3:p.Lys201Arg
XM_024448761.1:c.602A>G	XP_024304529.1:p.Lys201Arg
NM_003977.4:c.602A>G MANE Select	NP_003968.3:p.Lys201Arg
NM_001302960.2:c.602A>G	NP_001289889.1:p.Lys201Arg
NM_001302959.2:c.425A>G	NP_001289888.1:p.Lys142Arg