Canonical Allele Identifier: CA1980170071

Gene: AIP

Linked Data

• dbSNP Id: rs1865723027

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483052A>G , CM000673.2:g.67483052A>G	GRCh38
NC_000011.9:g.67250523A>G , CM000673.1:g.67250523A>G	GRCh37
NC_000011.8:g.67007099A>G	NCBI36
NG_008969.1:g.5019A>G , LRG_460:g.5019A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.-107A>G	ENSP00000434982.3:n.-107A>G
ENST00000682699.1:c.-107A>G	ENSP00000507935.1:n.-107A>G
ENST00000279146.8:c.-107A>G MANE Select	ENSP00000279146.3:n.-107A>G
ENST00000279146.7:c.-107A>G	ENSP00000279146.3:n.-107A>G
ENST00000528641.6:c.-107A>G	ENSP00000434982.2:n.-107A>G
ENST00000529797.1:n.4A>G
NM_001302960.1:c.-107A>G	NP_001289889.1:n.-107A>G
NM_003977.3:c.-107A>G	NP_003968.3:n.-107A>G
XM_024448761.1:c.-107A>G	XP_024304529.1:n.-107A>G
NM_003977.4:c.-107A>G MANE Select	NP_003968.3:n.-107A>G
NM_001302960.2:c.-107A>G	NP_001289889.1:n.-107A>G