Canonical Allele Identifier: CA2574896178

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483140G>A , CM000673.2:g.67483140G>A	GRCh38
NC_000011.9:g.67250611G>A , CM000673.1:g.67250611G>A	GRCh37
NC_000011.8:g.67007187G>A	NCBI36
NG_008969.1:g.5107G>A , LRG_460:g.5107G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000528641.7:c.-19G>A	ENSP00000434982.3:n.-19G>A
ENST00000682324.1:c.-19G>A	ENSP00000508017.1:n.-19G>A
ENST00000682699.1:c.-19G>A	ENSP00000507935.1:n.-19G>A
ENST00000683237.1:c.-19G>A	ENSP00000507343.1:n.-19G>A
ENST00000684006.1:c.-19G>A	ENSP00000507269.1:n.-19G>A
ENST00000684657.1:c.-19G>A	ENSP00000507961.1:n.-19G>A
ENST00000279146.8:c.-19G>A MANE Select	ENSP00000279146.3:n.-19G>A
ENST00000279146.7:c.-19G>A	ENSP00000279146.3:n.-19G>A
ENST00000528641.6:c.-19G>A	ENSP00000434982.2:n.-19G>A
ENST00000529797.1:n.92G>A
NM_001302960.1:c.-19G>A	NP_001289889.1:n.-19G>A
NM_003977.3:c.-19G>A	NP_003968.3:n.-19G>A
XM_024448761.1:c.-19G>A	XP_024304529.1:n.-19G>A
NM_003977.4:c.-19G>A MANE Select	NP_003968.3:n.-19G>A
NM_001302960.2:c.-19G>A	NP_001289889.1:n.-19G>A