Canonical Allele Identifier: CA6141006

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490935G>A , CM000673.2:g.67490935G>A	GRCh38
NC_000011.9:g.67258406G>A , CM000673.1:g.67258406G>A	GRCh37
NC_000011.8:g.67014982G>A	NCBI36
NG_008969.1:g.12902G>A , LRG_460:g.12902G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.935G>A MANE Select	NP_003968.3:p.Arg312Gln
ENST00000279146.8:c.935G>A MANE Select	ENSP00000279146.3:p.Arg312Gln
NM_001302959.1:c.758G>A	NP_001289888.1:p.Arg253Gln
NM_001302959.2:c.758G>A	NP_001289888.1:p.Arg253Gln
NM_001302960.1:c.*75G>A	NP_001289889.1:n.*75G>A
NM_001302960.2:c.*75G>A	NP_001289889.1:n.*75G>A
NM_003977.3:c.935G>A	NP_003968.3:p.Arg312Gln
ENST00000279146.7:c.935G>A	ENSP00000279146.3:p.Arg312Gln
ENST00000525341.2:c.1242G>A
ENST00000528641.7:c.746G>A	ENSP00000434982.3:p.Arg249Gln
ENST00000529797.2:n.1777G>A
ENST00000682324.1:c.469-62G>A	ENSP00000508017.1:n.469-62G>A
ENST00000682659.1:c.566G>A	ENSP00000507351.1:p.Arg189Gln
ENST00000682699.1:c.935G>A	ENSP00000507935.1:p.Arg312Gln
ENST00000683237.1:c.*75G>A	ENSP00000507343.1:n.*75G>A
ENST00000683856.1:c.758G>A	ENSP00000507979.1:p.Arg253Gln
ENST00000684006.1:c.*75G>A	ENSP00000507269.1:n.*75G>A
ENST00000684657.1:c.755G>A	ENSP00000507961.1:p.Arg252Gln
XM_024448761.1:c.935G>A	XP_024304529.1:p.Arg312Gln