Canonical Allele Identifier: CA224160811

Gene: AIP

Linked Data

• ClinVar Variation Id: 1798666
• ClinVar RCV Id: RCV002435637 ; RCV002469479
• dbSNP Id: rs377710724
• gnomAD v4: 11-67483157-G-A
• MyVariant Identifiers: chr11:g.67250628G>A (hg19) ; chr11:g.67483157G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483157G>A , CM000673.2:g.67483157G>A	GRCh38
NC_000011.9:g.67250628G>A , CM000673.1:g.67250628G>A	GRCh37
NC_000011.8:g.67007204G>A	NCBI36
NG_008969.1:g.5124G>A , LRG_460:g.5124G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.-2G>A	ENSP00000434982.3:n.-2G>A
ENST00000682324.1:c.-2G>A	ENSP00000508017.1:n.-2G>A
ENST00000682659.1:c.-2G>A	ENSP00000507351.1:n.-2G>A
ENST00000682699.1:c.-2G>A	ENSP00000507935.1:n.-2G>A
ENST00000683237.1:c.-2G>A	ENSP00000507343.1:n.-2G>A
ENST00000684006.1:c.-2G>A	ENSP00000507269.1:n.-2G>A
ENST00000684657.1:c.-2G>A	ENSP00000507961.1:n.-2G>A
ENST00000279146.8:c.-2G>A MANE Select	ENSP00000279146.3:n.-2G>A
ENST00000279146.7:c.-2G>A	ENSP00000279146.3:n.-2G>A
ENST00000528641.6:c.-2G>A	ENSP00000434982.2:n.-2G>A
ENST00000529797.1:n.109G>A
NM_001302960.1:c.-2G>A	NP_001289889.1:n.-2G>A
NM_003977.3:c.-2G>A	NP_003968.3:n.-2G>A
XM_024448761.1:c.-2G>A	XP_024304529.1:n.-2G>A
NM_003977.4:c.-2G>A MANE Select	NP_003968.3:n.-2G>A
NM_001302960.2:c.-2G>A	NP_001289889.1:n.-2G>A