Canonical Allele Identifier: CA381551470

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257789A>C (hg19) ; chr11:g.67490318A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490318A>C , CM000673.2:g.67490318A>C	GRCh38
NC_000011.9:g.67257789A>C , CM000673.1:g.67257789A>C	GRCh37
NC_000011.8:g.67014365A>C	NCBI36
NG_008969.1:g.12285A>C , LRG_460:g.12285A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.625A>C
ENST00000528641.7:c.459A>C	ENSP00000434982.3:p.Glu153Asp
ENST00000529797.2:n.1160A>C
ENST00000682324.1:c.469-679A>C	ENSP00000508017.1:n.469-679A>C
ENST00000682659.1:c.279A>C	ENSP00000507351.1:p.Glu93Asp
ENST00000682699.1:c.648A>C	ENSP00000507935.1:p.Glu216Asp
ENST00000683237.1:c.648A>C	ENSP00000507343.1:p.Glu216Asp
ENST00000683856.1:c.471A>C	ENSP00000507979.1:p.Glu157Asp
ENST00000684006.1:c.648A>C	ENSP00000507269.1:p.Glu216Asp
ENST00000684657.1:c.468A>C	ENSP00000507961.1:p.Glu156Asp
ENST00000279146.8:c.648A>C MANE Select	ENSP00000279146.3:p.Glu216Asp
ENST00000279146.7:c.648A>C	ENSP00000279146.3:p.Glu216Asp
ENST00000525341.1:c.300A>C	ENSP00000476993.1:p.Glu100Asp
ENST00000528641.6:c.459A>C	ENSP00000434982.2:p.Glu153Asp
NM_001302959.1:c.471A>C	NP_001289888.1:p.Glu157Asp
NM_001302960.1:c.648A>C	NP_001289889.1:p.Glu216Asp
NM_003977.3:c.648A>C	NP_003968.3:p.Glu216Asp
XM_024448761.1:c.648A>C	XP_024304529.1:p.Glu216Asp
NM_003977.4:c.648A>C MANE Select	NP_003968.3:p.Glu216Asp
NM_001302960.2:c.648A>C	NP_001289889.1:p.Glu216Asp
NM_001302959.2:c.471A>C	NP_001289888.1:p.Glu157Asp