Canonical Allele Identifier: CA939069909

Gene: AIP

Linked Data

• ClinVar Variation Id: 2717432
• ClinVar RCV Id: RCV003548787
• dbSNP Id: rs1865892536
• gnomAD v4: 11-67490779-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490779C>T , CM000673.2:g.67490779C>T	GRCh38
NC_000011.9:g.67258250C>T , CM000673.1:g.67258250C>T	GRCh37
NC_000011.8:g.67014826C>T	NCBI36
NG_008969.1:g.12746C>T , LRG_460:g.12746C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1086C>T
ENST00000528641.7:c.599-9C>T	ENSP00000434982.3:n.599-9C>T
ENST00000529797.2:n.1621C>T
ENST00000682324.1:c.469-218C>T	ENSP00000508017.1:n.469-218C>T
ENST00000682659.1:c.419-9C>T	ENSP00000507351.1:n.419-9C>T
ENST00000682699.1:c.788-9C>T	ENSP00000507935.1:n.788-9C>T
ENST00000683237.1:c.780-9C>T	ENSP00000507343.1:n.780-9C>T
ENST00000683856.1:c.611-9C>T	ENSP00000507979.1:n.611-9C>T
ENST00000684006.1:c.788-20C>T	ENSP00000507269.1:n.788-20C>T
ENST00000684657.1:c.608-9C>T	ENSP00000507961.1:n.608-9C>T
ENST00000279146.8:c.788-9C>T MANE Select	ENSP00000279146.3:n.788-9C>T
ENST00000279146.7:c.788-9C>T	ENSP00000279146.3:n.788-9C>T
ENST00000528641.6:c.599-9C>T	ENSP00000434982.2:n.599-9C>T
NM_001302959.1:c.611-9C>T	NP_001289888.1:n.611-9C>T
NM_001302960.1:c.780-9C>T	NP_001289889.1:n.780-9C>T
NM_003977.3:c.788-9C>T	NP_003968.3:n.788-9C>T
XM_024448761.1:c.788-9C>T	XP_024304529.1:n.788-9C>T
NM_003977.4:c.788-9C>T MANE Select	NP_003968.3:n.788-9C>T
NM_001302960.2:c.780-9C>T	NP_001289889.1:n.780-9C>T
NM_001302959.2:c.611-9C>T	NP_001289888.1:n.611-9C>T