Canonical Allele Identifier: CA381551217

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257658T>G (hg19) ; chr11:g.67490187T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490187T>G , CM000673.2:g.67490187T>G	GRCh38
NC_000011.9:g.67257658T>G , CM000673.1:g.67257658T>G	GRCh37
NC_000011.8:g.67014234T>G	NCBI36
NG_008969.1:g.12154T>G , LRG_460:g.12154T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.595T>G
ENST00000528641.7:c.429T>G	ENSP00000434982.3:p.Ile143Met
ENST00000529797.2:n.1130T>G
ENST00000682324.1:c.468+732T>G	ENSP00000508017.1:n.468+732T>G
ENST00000682659.1:c.249T>G	ENSP00000507351.1:p.Ile83Met
ENST00000682699.1:c.618T>G	ENSP00000507935.1:p.Ile206Met
ENST00000683237.1:c.618T>G	ENSP00000507343.1:p.Ile206Met
ENST00000683856.1:c.441T>G	ENSP00000507979.1:p.Ile147Met
ENST00000684006.1:c.618T>G	ENSP00000507269.1:p.Ile206Met
ENST00000684657.1:c.438T>G	ENSP00000507961.1:p.Ile146Met
ENST00000279146.8:c.618T>G MANE Select	ENSP00000279146.3:p.Ile206Met
ENST00000279146.7:c.618T>G	ENSP00000279146.3:p.Ile206Met
ENST00000525341.1:c.270T>G	ENSP00000476993.1:p.Ile90Met
ENST00000528641.6:c.429T>G	ENSP00000434982.2:p.Ile143Met
NM_001302959.1:c.441T>G	NP_001289888.1:p.Ile147Met
NM_001302960.1:c.618T>G	NP_001289889.1:p.Ile206Met
NM_003977.3:c.618T>G	NP_003968.3:p.Ile206Met
XM_024448761.1:c.618T>G	XP_024304529.1:p.Ile206Met
NM_003977.4:c.618T>G MANE Select	NP_003968.3:p.Ile206Met
NM_001302960.2:c.618T>G	NP_001289889.1:p.Ile206Met
NM_001302959.2:c.441T>G	NP_001289888.1:p.Ile147Met