Canonical Allele Identifier: CA381551946

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257922T>G (hg19) ; chr11:g.67490451T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490451T>G , CM000673.2:g.67490451T>G	GRCh38
NC_000011.9:g.67257922T>G , CM000673.1:g.67257922T>G	GRCh37
NC_000011.8:g.67014498T>G	NCBI36
NG_008969.1:g.12418T>G , LRG_460:g.12418T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.758T>G
ENST00000528641.7:c.592T>G	ENSP00000434982.3:p.Tyr198Asp
ENST00000529797.2:n.1293T>G
ENST00000682324.1:c.469-546T>G	ENSP00000508017.1:n.469-546T>G
ENST00000682659.1:c.412T>G	ENSP00000507351.1:p.Tyr138Asp
ENST00000682699.1:c.781T>G	ENSP00000507935.1:p.Tyr261Asp
ENST00000683237.1:c.779+2T>G	ENSP00000507343.1:n.779+2T>G
ENST00000683856.1:c.604T>G	ENSP00000507979.1:p.Tyr202Asp
ENST00000684006.1:c.781T>G	ENSP00000507269.1:p.Tyr261Asp
ENST00000684657.1:c.601T>G	ENSP00000507961.1:p.Tyr201Asp
ENST00000279146.8:c.781T>G MANE Select	ENSP00000279146.3:p.Tyr261Asp
ENST00000279146.7:c.781T>G	ENSP00000279146.3:p.Tyr261Asp
ENST00000525341.1:c.433T>G	ENSP00000476993.1:p.Tyr145Asp
ENST00000528641.6:c.592T>G	ENSP00000434982.2:p.Tyr198Asp
NM_001302959.1:c.604T>G	NP_001289888.1:p.Tyr202Asp
NM_001302960.1:c.779+2T>G	NP_001289889.1:n.779+2T>G
NM_003977.3:c.781T>G	NP_003968.3:p.Tyr261Asp
XM_024448761.1:c.781T>G	XP_024304529.1:p.Tyr261Asp
NM_003977.4:c.781T>G MANE Select	NP_003968.3:p.Tyr261Asp
NM_001302960.2:c.779+2T>G	NP_001289889.1:n.779+2T>G
NM_001302959.2:c.604T>G	NP_001289888.1:p.Tyr202Asp