Canonical Allele Identifier: CA475509244

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257637T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490166T>G , CM000673.2:g.67490166T>G	GRCh38
NC_000011.9:g.67257637T>G , CM000673.1:g.67257637T>G	GRCh37
NC_000011.8:g.67014213T>G	NCBI36
NG_008969.1:g.12133T>G , LRG_460:g.12133T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.574T>G
ENST00000528641.7:c.408T>G	ENSP00000434982.3:p.Ala136=
ENST00000529797.2:n.1109T>G
ENST00000682324.1:c.468+711T>G	ENSP00000508017.1:n.468+711T>G
ENST00000682659.1:c.228T>G	ENSP00000507351.1:p.Ala76=
ENST00000682699.1:c.597T>G	ENSP00000507935.1:p.Ala199=
ENST00000683237.1:c.597T>G	ENSP00000507343.1:p.Ala199=
ENST00000683856.1:c.420T>G	ENSP00000507979.1:p.Ala140=
ENST00000684006.1:c.597T>G	ENSP00000507269.1:p.Ala199=
ENST00000684657.1:c.417T>G	ENSP00000507961.1:p.Ala139=
ENST00000279146.8:c.597T>G MANE Select	ENSP00000279146.3:p.Ala199=
ENST00000279146.7:c.597T>G	ENSP00000279146.3:p.Ala199=
ENST00000525341.1:c.249T>G	ENSP00000476993.1:p.Ala83=
ENST00000528641.6:c.408T>G	ENSP00000434982.2:p.Ala136=
NM_001302959.1:c.420T>G	NP_001289888.1:p.Ala140=
NM_001302960.1:c.597T>G	NP_001289889.1:p.Ala199=
NM_003977.3:c.597T>G	NP_003968.3:p.Ala199=
XM_024448761.1:c.597T>G	XP_024304529.1:p.Ala199=
NM_003977.4:c.597T>G MANE Select	NP_003968.3:p.Ala199=
NM_001302960.2:c.597T>G	NP_001289889.1:p.Ala199=
NM_001302959.2:c.420T>G	NP_001289888.1:p.Ala140=