Canonical Allele Identifier: CA1139662056

Gene: AIP

Linked Data

• ClinVar Variation Id: 879697
• ClinVar RCV Id: RCV001107397
• dbSNP Id: rs1565180279
• gnomAD v4: 11-67483074-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483074C>T , CM000673.2:g.67483074C>T	GRCh38
NC_000011.9:g.67250545C>T , CM000673.1:g.67250545C>T	GRCh37
NC_000011.8:g.67007121C>T	NCBI36
NG_008969.1:g.5041C>T , LRG_460:g.5041C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.-85C>T	ENSP00000434982.3:n.-85C>T
ENST00000682324.1:c.-85C>T	ENSP00000508017.1:n.-85C>T
ENST00000682699.1:c.-85C>T	ENSP00000507935.1:n.-85C>T
ENST00000683237.1:c.-85C>T	ENSP00000507343.1:n.-85C>T
ENST00000684006.1:c.-85C>T	ENSP00000507269.1:n.-85C>T
ENST00000684657.1:c.-85C>T	ENSP00000507961.1:n.-85C>T
ENST00000279146.8:c.-85C>T MANE Select	ENSP00000279146.3:n.-85C>T
ENST00000279146.7:c.-85C>T	ENSP00000279146.3:n.-85C>T
ENST00000528641.6:c.-85C>T	ENSP00000434982.2:n.-85C>T
ENST00000529797.1:n.26C>T
NM_001302960.1:c.-85C>T	NP_001289889.1:n.-85C>T
NM_003977.3:c.-85C>T	NP_003968.3:n.-85C>T
XM_024448761.1:c.-85C>T	XP_024304529.1:n.-85C>T
NM_003977.4:c.-85C>T MANE Select	NP_003968.3:n.-85C>T
NM_001302960.2:c.-85C>T	NP_001289889.1:n.-85C>T