Canonical Allele Identifier: CA381554355

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258271C>A (hg19) ; chr11:g.67490800C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490800C>A , CM000673.2:g.67490800C>A	GRCh38
NC_000011.9:g.67258271C>A , CM000673.1:g.67258271C>A	GRCh37
NC_000011.8:g.67014847C>A	NCBI36
NG_008969.1:g.12767C>A , LRG_460:g.12767C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1107C>A
ENST00000528641.7:c.611C>A	ENSP00000434982.3:p.Ala204Asp
ENST00000529797.2:n.1642C>A
ENST00000682324.1:c.469-197C>A	ENSP00000508017.1:n.469-197C>A
ENST00000682659.1:c.431C>A	ENSP00000507351.1:p.Ala144Asp
ENST00000682699.1:c.800C>A	ENSP00000507935.1:p.Ala267Asp
ENST00000683237.1:c.792C>A	ENSP00000507343.1:p.Gly264=
ENST00000683856.1:c.623C>A	ENSP00000507979.1:p.Ala208Asp
ENST00000684006.1:c.789C>A	ENSP00000507269.1:p.Gly263=
ENST00000684657.1:c.620C>A	ENSP00000507961.1:p.Ala207Asp
ENST00000279146.8:c.800C>A MANE Select	ENSP00000279146.3:p.Ala267Asp
ENST00000279146.7:c.800C>A	ENSP00000279146.3:p.Ala267Asp
ENST00000528641.6:c.611C>A	ENSP00000434982.2:p.Ala204Asp
NM_001302959.1:c.623C>A	NP_001289888.1:p.Ala208Asp
NM_001302960.1:c.792C>A	NP_001289889.1:p.Gly264=
NM_003977.3:c.800C>A	NP_003968.3:p.Ala267Asp
XM_024448761.1:c.800C>A	XP_024304529.1:p.Ala267Asp
NM_003977.4:c.800C>A MANE Select	NP_003968.3:p.Ala267Asp
NM_001302960.2:c.792C>A	NP_001289889.1:p.Gly264=
NM_001302959.2:c.623C>A	NP_001289888.1:p.Ala208Asp