Canonical Allele Identifier: CA381551170

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257651A>C (hg19) ; chr11:g.67490180A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490180A>C , CM000673.2:g.67490180A>C	GRCh38
NC_000011.9:g.67257651A>C , CM000673.1:g.67257651A>C	GRCh37
NC_000011.8:g.67014227A>C	NCBI36
NG_008969.1:g.12147A>C , LRG_460:g.12147A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.588A>C
ENST00000528641.7:c.422A>C	ENSP00000434982.3:p.Asp141Ala
ENST00000529797.2:n.1123A>C
ENST00000682324.1:c.468+725A>C	ENSP00000508017.1:n.468+725A>C
ENST00000682659.1:c.242A>C	ENSP00000507351.1:p.Asp81Ala
ENST00000682699.1:c.611A>C	ENSP00000507935.1:p.Asp204Ala
ENST00000683237.1:c.611A>C	ENSP00000507343.1:p.Asp204Ala
ENST00000683856.1:c.434A>C	ENSP00000507979.1:p.Asp145Ala
ENST00000684006.1:c.611A>C	ENSP00000507269.1:p.Asp204Ala
ENST00000684657.1:c.431A>C	ENSP00000507961.1:p.Asp144Ala
ENST00000279146.8:c.611A>C MANE Select	ENSP00000279146.3:p.Asp204Ala
ENST00000279146.7:c.611A>C	ENSP00000279146.3:p.Asp204Ala
ENST00000525341.1:c.263A>C	ENSP00000476993.1:p.Asp88Ala
ENST00000528641.6:c.422A>C	ENSP00000434982.2:p.Asp141Ala
NM_001302959.1:c.434A>C	NP_001289888.1:p.Asp145Ala
NM_001302960.1:c.611A>C	NP_001289889.1:p.Asp204Ala
NM_003977.3:c.611A>C	NP_003968.3:p.Asp204Ala
XM_024448761.1:c.611A>C	XP_024304529.1:p.Asp204Ala
NM_003977.4:c.611A>C MANE Select	NP_003968.3:p.Asp204Ala
NM_001302960.2:c.611A>C	NP_001289889.1:p.Asp204Ala
NM_001302959.2:c.434A>C	NP_001289888.1:p.Asp145Ala