Canonical Allele Identifier: CA381555522

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258453T>G (hg19) ; chr11:g.67490982T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490982T>G , CM000673.2:g.67490982T>G	GRCh38
NC_000011.9:g.67258453T>G , CM000673.1:g.67258453T>G	GRCh37
NC_000011.8:g.67015029T>G	NCBI36
NG_008969.1:g.12949T>G , LRG_460:g.12949T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1289T>G
ENST00000528641.7:c.793T>G	ENSP00000434982.3:p.Phe265Val
ENST00000529797.2:n.1824T>G
ENST00000682324.1:c.469-15T>G	ENSP00000508017.1:n.469-15T>G
ENST00000682659.1:c.613T>G	ENSP00000507351.1:p.Phe205Val
ENST00000683237.1:c.*122T>G	ENSP00000507343.1:n.*122T>G
ENST00000683856.1:c.805T>G	ENSP00000507979.1:p.Phe269Val
ENST00000684006.1:c.*122T>G	ENSP00000507269.1:n.*122T>G
ENST00000684657.1:c.802T>G	ENSP00000507961.1:p.Phe268Val
ENST00000279146.8:c.982T>G MANE Select	ENSP00000279146.3:p.Phe328Val
ENST00000279146.7:c.982T>G	ENSP00000279146.3:p.Phe328Val
NM_001302959.1:c.805T>G	NP_001289888.1:p.Phe269Val
NM_001302960.1:c.*122T>G	NP_001289889.1:n.*122T>G
NM_003977.3:c.982T>G	NP_003968.3:p.Phe328Val
XM_024448761.1:c.982T>G	XP_024304529.1:p.Phe328Val
NM_003977.4:c.982T>G MANE Select	NP_003968.3:p.Phe328Val
NM_001302960.2:c.*122T>G	NP_001289889.1:n.*122T>G
NM_001302959.2:c.805T>G	NP_001289888.1:p.Phe269Val