Canonical Allele Identifier: CA381551923

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257912C>G (hg19) ; chr11:g.67490441C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490441C>G , CM000673.2:g.67490441C>G	GRCh38
NC_000011.9:g.67257912C>G , CM000673.1:g.67257912C>G	GRCh37
NC_000011.8:g.67014488C>G	NCBI36
NG_008969.1:g.12408C>G , LRG_460:g.12408C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.748C>G
ENST00000528641.7:c.582C>G	ENSP00000434982.3:p.Ile194Met
ENST00000529797.2:n.1283C>G
ENST00000682324.1:c.469-556C>G	ENSP00000508017.1:n.469-556C>G
ENST00000682659.1:c.402C>G	ENSP00000507351.1:p.Ile134Met
ENST00000682699.1:c.771C>G	ENSP00000507935.1:p.Ile257Met
ENST00000683237.1:c.771C>G	ENSP00000507343.1:p.Ile257Met
ENST00000683856.1:c.594C>G	ENSP00000507979.1:p.Ile198Met
ENST00000684006.1:c.771C>G	ENSP00000507269.1:p.Ile257Met
ENST00000684657.1:c.591C>G	ENSP00000507961.1:p.Ile197Met
ENST00000279146.8:c.771C>G MANE Select	ENSP00000279146.3:p.Ile257Met
ENST00000279146.7:c.771C>G	ENSP00000279146.3:p.Ile257Met
ENST00000525341.1:c.423C>G	ENSP00000476993.1:p.Ile141Met
ENST00000528641.6:c.582C>G	ENSP00000434982.2:p.Ile194Met
NM_001302959.1:c.594C>G	NP_001289888.1:p.Ile198Met
NM_001302960.1:c.771C>G	NP_001289889.1:p.Ile257Met
NM_003977.3:c.771C>G	NP_003968.3:p.Ile257Met
XM_024448761.1:c.771C>G	XP_024304529.1:p.Ile257Met
NM_003977.4:c.771C>G MANE Select	NP_003968.3:p.Ile257Met
NM_001302960.2:c.771C>G	NP_001289889.1:p.Ile257Met
NM_001302959.2:c.594C>G	NP_001289888.1:p.Ile198Met