Canonical Allele Identifier: CA224166163

Gene: AIP

Linked Data

• dbSNP Id: rs959182919
• gnomAD v4: 11-67491042-C-T
• MyVariant Identifiers: chr11:g.67258513C>T (hg19) ; chr11:g.67491042C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67491042C>T , CM000673.2:g.67491042C>T	GRCh38
NC_000011.9:g.67258513C>T , CM000673.1:g.67258513C>T	GRCh37
NC_000011.8:g.67015089C>T	NCBI36
NG_008969.1:g.13009C>T , LRG_460:g.13009C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.*49C>T	ENSP00000434982.3:n.*49C>T
ENST00000529797.2:n.1884C>T
ENST00000682324.1:c.514C>T	ENSP00000508017.1:p.Pro172Ser
ENST00000682659.1:c.*49C>T	ENSP00000507351.1:n.*49C>T
ENST00000683237.1:c.*182C>T	ENSP00000507343.1:n.*182C>T
ENST00000683856.1:c.*49C>T	ENSP00000507979.1:n.*49C>T
ENST00000684006.1:c.*182C>T	ENSP00000507269.1:n.*182C>T
ENST00000684657.1:c.*49C>T	ENSP00000507961.1:n.*49C>T
ENST00000279146.8:c.*49C>T MANE Select	ENSP00000279146.3:n.*49C>T
ENST00000279146.7:c.*49C>T	ENSP00000279146.3:n.*49C>T
NM_001302959.1:c.*49C>T	NP_001289888.1:n.*49C>T
NM_001302960.1:c.*182C>T	NP_001289889.1:n.*182C>T
NM_003977.3:c.*49C>T	NP_003968.3:n.*49C>T
XM_024448761.1:c.*49C>T	XP_024304529.1:n.*49C>T
NM_003977.4:c.*49C>T MANE Select	NP_003968.3:n.*49C>T
NM_001302960.2:c.*182C>T	NP_001289889.1:n.*182C>T
NM_001302959.2:c.*49C>T	NP_001289888.1:n.*49C>T