Canonical Allele Identifier: CA381554269

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258260C>G (hg19) ; chr11:g.67490789C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490789C>G , CM000673.2:g.67490789C>G	GRCh38
NC_000011.9:g.67258260C>G , CM000673.1:g.67258260C>G	GRCh37
NC_000011.8:g.67014836C>G	NCBI36
NG_008969.1:g.12756C>G , LRG_460:g.12756C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1096C>G
ENST00000528641.7:c.600C>G	ENSP00000434982.3:p.Asp200Glu
ENST00000529797.2:n.1631C>G
ENST00000682324.1:c.469-208C>G	ENSP00000508017.1:n.469-208C>G
ENST00000682659.1:c.420C>G	ENSP00000507351.1:p.Asp140Glu
ENST00000682699.1:c.789C>G	ENSP00000507935.1:p.Asp263Glu
ENST00000683237.1:c.781C>G	ENSP00000507343.1:p.Gln261Glu
ENST00000683856.1:c.612C>G	ENSP00000507979.1:p.Asp204Glu
ENST00000684006.1:c.788-10C>G	ENSP00000507269.1:n.788-10C>G
ENST00000684657.1:c.609C>G	ENSP00000507961.1:p.Asp203Glu
ENST00000279146.8:c.789C>G MANE Select	ENSP00000279146.3:p.Asp263Glu
ENST00000279146.7:c.789C>G	ENSP00000279146.3:p.Asp263Glu
ENST00000528641.6:c.600C>G	ENSP00000434982.2:p.Asp200Glu
NM_001302959.1:c.612C>G	NP_001289888.1:p.Asp204Glu
NM_001302960.1:c.781C>G	NP_001289889.1:p.Gln261Glu
NM_003977.3:c.789C>G	NP_003968.3:p.Asp263Glu
XM_024448761.1:c.789C>G	XP_024304529.1:p.Asp263Glu
NM_003977.4:c.789C>G MANE Select	NP_003968.3:p.Asp263Glu
NM_001302960.2:c.781C>G	NP_001289889.1:p.Gln261Glu
NM_001302959.2:c.612C>G	NP_001289888.1:p.Asp204Glu