Canonical Allele Identifier: CA381554594

Gene: AIP

Linked Data

• gnomAD v4: 11-67490825-C-G
• MyVariant Identifiers: chr11:g.67258296C>G (hg19) ; chr11:g.67490825C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490825C>G , CM000673.2:g.67490825C>G	GRCh38
NC_000011.9:g.67258296C>G , CM000673.1:g.67258296C>G	GRCh37
NC_000011.8:g.67014872C>G	NCBI36
NG_008969.1:g.12792C>G , LRG_460:g.12792C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1132C>G
ENST00000528641.7:c.636C>G	ENSP00000434982.3:p.His212Gln
ENST00000529797.2:n.1667C>G
ENST00000682324.1:c.469-172C>G	ENSP00000508017.1:n.469-172C>G
ENST00000682659.1:c.456C>G	ENSP00000507351.1:p.His152Gln
ENST00000682699.1:c.825C>G	ENSP00000507935.1:p.His275Gln
ENST00000683237.1:c.817C>G	ENSP00000507343.1:p.Arg273Gly
ENST00000683856.1:c.648C>G	ENSP00000507979.1:p.His216Gln
ENST00000684006.1:c.814C>G	ENSP00000507269.1:p.Arg272Gly
ENST00000684657.1:c.645C>G	ENSP00000507961.1:p.His215Gln
ENST00000279146.8:c.825C>G MANE Select	ENSP00000279146.3:p.His275Gln
ENST00000279146.7:c.825C>G	ENSP00000279146.3:p.His275Gln
ENST00000528641.6:c.636C>G	ENSP00000434982.2:p.His212Gln
NM_001302959.1:c.648C>G	NP_001289888.1:p.His216Gln
NM_001302960.1:c.817C>G	NP_001289889.1:p.Arg273Gly
NM_003977.3:c.825C>G	NP_003968.3:p.His275Gln
XM_024448761.1:c.825C>G	XP_024304529.1:p.His275Gln
NM_003977.4:c.825C>G MANE Select	NP_003968.3:p.His275Gln
NM_001302960.2:c.817C>G	NP_001289889.1:p.Arg273Gly
NM_001302959.2:c.648C>G	NP_001289888.1:p.His216Gln