Canonical Allele Identifier: CA381554231

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258259A>G (hg19) ; chr11:g.67490788A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490788A>G , CM000673.2:g.67490788A>G	GRCh38
NC_000011.9:g.67258259A>G , CM000673.1:g.67258259A>G	GRCh37
NC_000011.8:g.67014835A>G	NCBI36
NG_008969.1:g.12755A>G , LRG_460:g.12755A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1095A>G
ENST00000528641.7:c.599A>G	ENSP00000434982.3:p.Asp200Gly
ENST00000529797.2:n.1630A>G
ENST00000682324.1:c.469-209A>G	ENSP00000508017.1:n.469-209A>G
ENST00000682659.1:c.419A>G	ENSP00000507351.1:p.Asp140Gly
ENST00000682699.1:c.788A>G	ENSP00000507935.1:p.Asp263Gly
ENST00000683237.1:c.780A>G	ENSP00000507343.1:p.Lys260=
ENST00000683856.1:c.611A>G	ENSP00000507979.1:p.Asp204Gly
ENST00000684006.1:c.788-11A>G	ENSP00000507269.1:n.788-11A>G
ENST00000684657.1:c.608A>G	ENSP00000507961.1:p.Asp203Gly
ENST00000279146.8:c.788A>G MANE Select	ENSP00000279146.3:p.Asp263Gly
ENST00000279146.7:c.788A>G	ENSP00000279146.3:p.Asp263Gly
ENST00000528641.6:c.599A>G	ENSP00000434982.2:p.Asp200Gly
NM_001302959.1:c.611A>G	NP_001289888.1:p.Asp204Gly
NM_001302960.1:c.780A>G	NP_001289889.1:p.Lys260=
NM_003977.3:c.788A>G	NP_003968.3:p.Asp263Gly
XM_024448761.1:c.788A>G	XP_024304529.1:p.Asp263Gly
NM_003977.4:c.788A>G MANE Select	NP_003968.3:p.Asp263Gly
NM_001302960.2:c.780A>G	NP_001289889.1:p.Lys260=
NM_001302959.2:c.611A>G	NP_001289888.1:p.Asp204Gly