Canonical Allele Identifier: CA1980172632

Gene: AIP

Linked Data

• ClinVar Variation Id: 1955729
• ClinVar RCV Id: RCV002695612
• dbSNP Id: rs1591047175

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490777C>G , CM000673.2:g.67490777C>G	GRCh38
NC_000011.9:g.67258248C>G , CM000673.1:g.67258248C>G	GRCh37
NC_000011.8:g.67014824C>G	NCBI36
NG_008969.1:g.12744C>G , LRG_460:g.12744C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1084C>G
ENST00000528641.7:c.599-11C>G	ENSP00000434982.3:n.599-11C>G
ENST00000529797.2:n.1619C>G
ENST00000682324.1:c.469-220C>G	ENSP00000508017.1:n.469-220C>G
ENST00000682659.1:c.419-11C>G	ENSP00000507351.1:n.419-11C>G
ENST00000682699.1:c.788-11C>G	ENSP00000507935.1:n.788-11C>G
ENST00000683237.1:c.780-11C>G	ENSP00000507343.1:n.780-11C>G
ENST00000683856.1:c.611-11C>G	ENSP00000507979.1:n.611-11C>G
ENST00000684006.1:c.788-22C>G	ENSP00000507269.1:n.788-22C>G
ENST00000684657.1:c.608-11C>G	ENSP00000507961.1:n.608-11C>G
ENST00000279146.8:c.788-11C>G MANE Select	ENSP00000279146.3:n.788-11C>G
ENST00000279146.7:c.788-11C>G	ENSP00000279146.3:n.788-11C>G
ENST00000528641.6:c.599-11C>G	ENSP00000434982.2:n.599-11C>G
NM_001302959.1:c.611-11C>G	NP_001289888.1:n.611-11C>G
NM_001302960.1:c.780-11C>G	NP_001289889.1:n.780-11C>G
NM_003977.3:c.788-11C>G	NP_003968.3:n.788-11C>G
XM_024448761.1:c.788-11C>G	XP_024304529.1:n.788-11C>G
NM_003977.4:c.788-11C>G MANE Select	NP_003968.3:n.788-11C>G
NM_001302960.2:c.780-11C>G	NP_001289889.1:n.780-11C>G
NM_001302959.2:c.611-11C>G	NP_001289888.1:n.611-11C>G