Canonical Allele Identifier: CA6141012

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490964G>A , CM000673.2:g.67490964G>A	GRCh38
NC_000011.9:g.67258435G>A , CM000673.1:g.67258435G>A	GRCh37
NC_000011.8:g.67015011G>A	NCBI36
NG_008969.1:g.12931G>A , LRG_460:g.12931G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.964G>A MANE Select	NP_003968.3:p.Ala322Thr
ENST00000279146.8:c.964G>A MANE Select	ENSP00000279146.3:p.Ala322Thr
NM_001302959.1:c.787G>A	NP_001289888.1:p.Ala263Thr
NM_001302959.2:c.787G>A	NP_001289888.1:p.Ala263Thr
NM_001302960.1:c.*104G>A	NP_001289889.1:n.*104G>A
NM_001302960.2:c.*104G>A	NP_001289889.1:n.*104G>A
NM_003977.3:c.964G>A	NP_003968.3:p.Ala322Thr
ENST00000279146.7:c.964G>A	ENSP00000279146.3:p.Ala322Thr
ENST00000525341.2:c.1271G>A
ENST00000528641.7:c.775G>A	ENSP00000434982.3:p.Ala259Thr
ENST00000529797.2:n.1806G>A
ENST00000682324.1:c.469-33G>A	ENSP00000508017.1:n.469-33G>A
ENST00000682659.1:c.595G>A	ENSP00000507351.1:p.Ala199Thr
ENST00000683237.1:c.*104G>A	ENSP00000507343.1:n.*104G>A
ENST00000683856.1:c.787G>A	ENSP00000507979.1:p.Ala263Thr
ENST00000684006.1:c.*104G>A	ENSP00000507269.1:n.*104G>A
ENST00000684657.1:c.784G>A	ENSP00000507961.1:p.Ala262Thr
XM_024448761.1:c.964G>A	XP_024304529.1:p.Ala322Thr