Canonical Allele Identifier: CA381554403

Gene: AIP

Linked Data

• gnomAD v4: 11-67490804-C-G
• MyVariant Identifiers: chr11:g.67258275C>G (hg19) ; chr11:g.67490804C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490804C>G , CM000673.2:g.67490804C>G	GRCh38
NC_000011.9:g.67258275C>G , CM000673.1:g.67258275C>G	GRCh37
NC_000011.8:g.67014851C>G	NCBI36
NG_008969.1:g.12771C>G , LRG_460:g.12771C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1111C>G
ENST00000528641.7:c.615C>G	ENSP00000434982.3:p.Tyr205Ter
ENST00000529797.2:n.1646C>G
ENST00000682324.1:c.469-193C>G	ENSP00000508017.1:n.469-193C>G
ENST00000682659.1:c.435C>G	ENSP00000507351.1:p.Tyr145Ter
ENST00000682699.1:c.804C>G	ENSP00000507935.1:p.Tyr268Ter
ENST00000683237.1:c.796C>G	ENSP00000507343.1:p.Leu266Val
ENST00000683856.1:c.627C>G	ENSP00000507979.1:p.Tyr209Ter
ENST00000684006.1:c.793C>G	ENSP00000507269.1:p.Leu265Val
ENST00000684657.1:c.624C>G	ENSP00000507961.1:p.Tyr208Ter
ENST00000279146.8:c.804C>G MANE Select	ENSP00000279146.3:p.Tyr268Ter
ENST00000279146.7:c.804C>G	ENSP00000279146.3:p.Tyr268Ter
ENST00000528641.6:c.615C>G	ENSP00000434982.2:p.Tyr205Ter
NM_001302959.1:c.627C>G	NP_001289888.1:p.Tyr209Ter
NM_001302960.1:c.796C>G	NP_001289889.1:p.Leu266Val
NM_003977.3:c.804C>G	NP_003968.3:p.Tyr268Ter
XM_024448761.1:c.804C>G	XP_024304529.1:p.Tyr268Ter
NM_003977.4:c.804C>G MANE Select	NP_003968.3:p.Tyr268Ter
NM_001302960.2:c.796C>G	NP_001289889.1:p.Leu266Val
NM_001302959.2:c.627C>G	NP_001289888.1:p.Tyr209Ter