Canonical Allele Identifier: CA381555132

Gene: AIP

Linked Data

• dbSNP Id: rs1157839241
• gnomAD v2: 11-67258355-A-G
• gnomAD v4: 11-67490884-A-G
• MyVariant Identifiers: chr11:g.67258355A>G (hg19) ; chr11:g.67490884A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490884A>G , CM000673.2:g.67490884A>G	GRCh38
NC_000011.9:g.67258355A>G , CM000673.1:g.67258355A>G	GRCh37
NC_000011.8:g.67014931A>G	NCBI36
NG_008969.1:g.12851A>G , LRG_460:g.12851A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1191A>G
ENST00000528641.7:c.695A>G	ENSP00000434982.3:p.Asp232Gly
ENST00000529797.2:n.1726A>G
ENST00000682324.1:c.469-113A>G	ENSP00000508017.1:n.469-113A>G
ENST00000682659.1:c.515A>G	ENSP00000507351.1:p.Asp172Gly
ENST00000682699.1:c.884A>G	ENSP00000507935.1:p.Asp295Gly
ENST00000683237.1:c.*24A>G	ENSP00000507343.1:n.*24A>G
ENST00000683856.1:c.707A>G	ENSP00000507979.1:p.Asp236Gly
ENST00000684006.1:c.*24A>G	ENSP00000507269.1:n.*24A>G
ENST00000684657.1:c.704A>G	ENSP00000507961.1:p.Asp235Gly
ENST00000279146.8:c.884A>G MANE Select	ENSP00000279146.3:p.Asp295Gly
ENST00000279146.7:c.884A>G	ENSP00000279146.3:p.Asp295Gly
ENST00000528641.6:c.695A>G	ENSP00000434982.2:p.Asp232Gly
NM_001302959.1:c.707A>G	NP_001289888.1:p.Asp236Gly
NM_001302960.1:c.*24A>G	NP_001289889.1:n.*24A>G
NM_003977.3:c.884A>G	NP_003968.3:p.Asp295Gly
XM_024448761.1:c.884A>G	XP_024304529.1:p.Asp295Gly
NM_003977.4:c.884A>G MANE Select	NP_003968.3:p.Asp295Gly
NM_001302960.2:c.*24A>G	NP_001289889.1:n.*24A>G
NM_001302959.2:c.707A>G	NP_001289888.1:p.Asp236Gly