Canonical Allele Identifier: CA381551580

Gene: AIP

Linked Data

• ClinVar Variation Id: 1755672
• ClinVar RCV Id: RCV002369640
• MyVariant Identifiers: chr11:g.67257823C>G (hg19) ; chr11:g.67490352C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490352C>G , CM000673.2:g.67490352C>G	GRCh38
NC_000011.9:g.67257823C>G , CM000673.1:g.67257823C>G	GRCh37
NC_000011.8:g.67014399C>G	NCBI36
NG_008969.1:g.12319C>G , LRG_460:g.12319C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.659C>G
ENST00000528641.7:c.493C>G	ENSP00000434982.3:p.Gln165Glu
ENST00000529797.2:n.1194C>G
ENST00000682324.1:c.469-645C>G	ENSP00000508017.1:n.469-645C>G
ENST00000682659.1:c.313C>G	ENSP00000507351.1:p.Gln105Glu
ENST00000682699.1:c.682C>G	ENSP00000507935.1:p.Gln228Glu
ENST00000683237.1:c.682C>G	ENSP00000507343.1:p.Gln228Glu
ENST00000683856.1:c.505C>G	ENSP00000507979.1:p.Gln169Glu
ENST00000684006.1:c.682C>G	ENSP00000507269.1:p.Gln228Glu
ENST00000684657.1:c.502C>G	ENSP00000507961.1:p.Gln168Glu
ENST00000279146.8:c.682C>G MANE Select	ENSP00000279146.3:p.Gln228Glu
ENST00000279146.7:c.682C>G	ENSP00000279146.3:p.Gln228Glu
ENST00000525341.1:c.334C>G	ENSP00000476993.1:p.Gln112Glu
ENST00000528641.6:c.493C>G	ENSP00000434982.2:p.Gln165Glu
NM_001302959.1:c.505C>G	NP_001289888.1:p.Gln169Glu
NM_001302960.1:c.682C>G	NP_001289889.1:p.Gln228Glu
NM_003977.3:c.682C>G	NP_003968.3:p.Gln228Glu
XM_024448761.1:c.682C>G	XP_024304529.1:p.Gln228Glu
NM_003977.4:c.682C>G MANE Select	NP_003968.3:p.Gln228Glu
NM_001302960.2:c.682C>G	NP_001289889.1:p.Gln228Glu
NM_001302959.2:c.505C>G	NP_001289888.1:p.Gln169Glu