Canonical Allele Identifier: CA381546688

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487069G>A , CM000673.2:g.67487069G>A	GRCh38
NC_000011.9:g.67254540G>A , CM000673.1:g.67254540G>A	GRCh37
NC_000011.8:g.67011116G>A	NCBI36
NG_008969.1:g.9036G>A , LRG_460:g.9036G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.163G>A MANE Select	NP_003968.3:p.Ala55Thr
ENST00000279146.8:c.163G>A MANE Select	ENSP00000279146.3:p.Ala55Thr
NM_001302959.1:c.-15G>A	NP_001289888.1:n.-15G>A
NM_001302959.2:c.-15G>A	NP_001289888.1:n.-15G>A
NM_001302960.1:c.163G>A	NP_001289889.1:p.Ala55Thr
NM_001302960.2:c.163G>A	NP_001289889.1:p.Ala55Thr
NM_003977.3:c.163G>A	NP_003968.3:p.Ala55Thr
ENST00000279146.7:c.163G>A	ENSP00000279146.3:p.Ala55Thr
ENST00000525341.2:c.140G>A
ENST00000528641.6:c.163G>A	ENSP00000434982.2:p.Ala55Thr
ENST00000528641.7:c.163G>A	ENSP00000434982.3:p.Ala55Thr
ENST00000529797.1:n.273G>A
ENST00000529797.2:n.93G>A
ENST00000682324.1:c.163G>A	ENSP00000508017.1:p.Ala55Thr
ENST00000682659.1:c.100-2969G>A	ENSP00000507351.1:n.100-2969G>A
ENST00000682699.1:c.163G>A	ENSP00000507935.1:p.Ala55Thr
ENST00000683237.1:c.163G>A	ENSP00000507343.1:p.Ala55Thr
ENST00000683856.1:c.-15G>A	ENSP00000507979.1:n.-15G>A
ENST00000684006.1:c.163G>A	ENSP00000507269.1:p.Ala55Thr
ENST00000684657.1:c.100-2198G>A	ENSP00000507961.1:n.100-2198G>A
XM_024448761.1:c.163G>A	XP_024304529.1:p.Ala55Thr