Canonical Allele Identifier: CA381551190

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257654C>A (hg19) ; chr11:g.67490183C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490183C>A , CM000673.2:g.67490183C>A	GRCh38
NC_000011.9:g.67257654C>A , CM000673.1:g.67257654C>A	GRCh37
NC_000011.8:g.67014230C>A	NCBI36
NG_008969.1:g.12150C>A , LRG_460:g.12150C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.591C>A
ENST00000528641.7:c.425C>A	ENSP00000434982.3:p.Ala142Asp
ENST00000529797.2:n.1126C>A
ENST00000682324.1:c.468+728C>A	ENSP00000508017.1:n.468+728C>A
ENST00000682659.1:c.245C>A	ENSP00000507351.1:p.Ala82Asp
ENST00000682699.1:c.614C>A	ENSP00000507935.1:p.Ala205Asp
ENST00000683237.1:c.614C>A	ENSP00000507343.1:p.Ala205Asp
ENST00000683856.1:c.437C>A	ENSP00000507979.1:p.Ala146Asp
ENST00000684006.1:c.614C>A	ENSP00000507269.1:p.Ala205Asp
ENST00000684657.1:c.434C>A	ENSP00000507961.1:p.Ala145Asp
ENST00000279146.8:c.614C>A MANE Select	ENSP00000279146.3:p.Ala205Asp
ENST00000279146.7:c.614C>A	ENSP00000279146.3:p.Ala205Asp
ENST00000525341.1:c.266C>A	ENSP00000476993.1:p.Ala89Asp
ENST00000528641.6:c.425C>A	ENSP00000434982.2:p.Ala142Asp
NM_001302959.1:c.437C>A	NP_001289888.1:p.Ala146Asp
NM_001302960.1:c.614C>A	NP_001289889.1:p.Ala205Asp
NM_003977.3:c.614C>A	NP_003968.3:p.Ala205Asp
XM_024448761.1:c.614C>A	XP_024304529.1:p.Ala205Asp
NM_003977.4:c.614C>A MANE Select	NP_003968.3:p.Ala205Asp
NM_001302960.2:c.614C>A	NP_001289889.1:p.Ala205Asp
NM_001302959.2:c.437C>A	NP_001289888.1:p.Ala146Asp