Canonical Allele Identifier: CA381550615

Gene: AIP

Linked Data

• gnomAD v4: 11-67490096-C-T
• MyVariant Identifiers: chr11:g.67257567C>T (hg19) ; chr11:g.67490096C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490096C>T , CM000673.2:g.67490096C>T	GRCh38
NC_000011.9:g.67257567C>T , CM000673.1:g.67257567C>T	GRCh37
NC_000011.8:g.67014143C>T	NCBI36
NG_008969.1:g.12063C>T , LRG_460:g.12063C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.504C>T
ENST00000528641.7:c.338C>T	ENSP00000434982.3:p.Ala113Val
ENST00000529797.2:n.1039C>T
ENST00000682324.1:c.468+641C>T	ENSP00000508017.1:n.468+641C>T
ENST00000682659.1:c.158C>T	ENSP00000507351.1:p.Ala53Val
ENST00000682699.1:c.527C>T	ENSP00000507935.1:p.Ala176Val
ENST00000683237.1:c.527C>T	ENSP00000507343.1:p.Ala176Val
ENST00000683856.1:c.350C>T	ENSP00000507979.1:p.Ala117Val
ENST00000684006.1:c.527C>T	ENSP00000507269.1:p.Ala176Val
ENST00000684657.1:c.347C>T	ENSP00000507961.1:p.Ala116Val
ENST00000279146.8:c.527C>T MANE Select	ENSP00000279146.3:p.Ala176Val
ENST00000279146.7:c.527C>T	ENSP00000279146.3:p.Ala176Val
ENST00000525341.1:c.179C>T	ENSP00000476993.1:p.Ala60Val
ENST00000528641.6:c.338C>T	ENSP00000434982.2:p.Ala113Val
NM_001302959.1:c.350C>T	NP_001289888.1:p.Ala117Val
NM_001302960.1:c.527C>T	NP_001289889.1:p.Ala176Val
NM_003977.3:c.527C>T	NP_003968.3:p.Ala176Val
XM_024448761.1:c.527C>T	XP_024304529.1:p.Ala176Val
NM_003977.4:c.527C>T MANE Select	NP_003968.3:p.Ala176Val
NM_001302960.2:c.527C>T	NP_001289889.1:p.Ala176Val
NM_001302959.2:c.350C>T	NP_001289888.1:p.Ala117Val