Canonical Allele Identifier: CA381555376

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258400A>C (hg19) ; chr11:g.67490929A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490929A>C , CM000673.2:g.67490929A>C	GRCh38
NC_000011.9:g.67258400A>C , CM000673.1:g.67258400A>C	GRCh37
NC_000011.8:g.67014976A>C	NCBI36
NG_008969.1:g.12896A>C , LRG_460:g.12896A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1236A>C
ENST00000528641.7:c.740A>C	ENSP00000434982.3:p.Glu247Ala
ENST00000529797.2:n.1771A>C
ENST00000682324.1:c.469-68A>C	ENSP00000508017.1:n.469-68A>C
ENST00000682659.1:c.560A>C	ENSP00000507351.1:p.Glu187Ala
ENST00000682699.1:c.929A>C	ENSP00000507935.1:p.Glu310Ala
ENST00000683237.1:c.*69A>C	ENSP00000507343.1:n.*69A>C
ENST00000683856.1:c.752A>C	ENSP00000507979.1:p.Glu251Ala
ENST00000684006.1:c.*69A>C	ENSP00000507269.1:n.*69A>C
ENST00000684657.1:c.749A>C	ENSP00000507961.1:p.Glu250Ala
ENST00000279146.8:c.929A>C MANE Select	ENSP00000279146.3:p.Glu310Ala
ENST00000279146.7:c.929A>C	ENSP00000279146.3:p.Glu310Ala
NM_001302959.1:c.752A>C	NP_001289888.1:p.Glu251Ala
NM_001302960.1:c.*69A>C	NP_001289889.1:n.*69A>C
NM_003977.3:c.929A>C	NP_003968.3:p.Glu310Ala
XM_024448761.1:c.929A>C	XP_024304529.1:p.Glu310Ala
NM_003977.4:c.929A>C MANE Select	NP_003968.3:p.Glu310Ala
NM_001302960.2:c.*69A>C	NP_001289889.1:n.*69A>C
NM_001302959.2:c.752A>C	NP_001289888.1:p.Glu251Ala