Canonical Allele Identifier: CA10639905

Gene: AIP

Linked Data

• ClinVar Variation Id: 305725
• ClinVar RCV Id: RCV000361473
• dbSNP Id: rs886048584
• MyVariant Identifiers: chr11:g.67254479C>G (hg19) ; chr11:g.67487008C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487008C>G , CM000673.2:g.67487008C>G	GRCh38
NC_000011.9:g.67254479C>G , CM000673.1:g.67254479C>G	GRCh37
NC_000011.8:g.67011055C>G	NCBI36
NG_008969.1:g.8975C>G , LRG_460:g.8975C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.79C>G
ENST00000528641.7:c.102C>G	ENSP00000434982.3:p.Ala34=
ENST00000529797.2:n.32C>G
ENST00000682324.1:c.102C>G	ENSP00000508017.1:p.Ala34=
ENST00000682659.1:c.100-3030C>G	ENSP00000507351.1:n.100-3030C>G
ENST00000682699.1:c.102C>G	ENSP00000507935.1:p.Ala34=
ENST00000683237.1:c.102C>G	ENSP00000507343.1:p.Ala34=
ENST00000683856.1:c.-76C>G	ENSP00000507979.1:n.-76C>G
ENST00000684006.1:c.102C>G	ENSP00000507269.1:p.Ala34=
ENST00000684657.1:c.100-2259C>G	ENSP00000507961.1:n.100-2259C>G
ENST00000279146.8:c.102C>G MANE Select	ENSP00000279146.3:p.Ala34=
ENST00000279146.7:c.102C>G	ENSP00000279146.3:p.Ala34=
ENST00000528641.6:c.102C>G	ENSP00000434982.2:p.Ala34=
ENST00000529797.1:n.212C>G
NM_001302959.1:c.-76C>G	NP_001289888.1:n.-76C>G
NM_001302960.1:c.102C>G	NP_001289889.1:p.Ala34=
NM_003977.3:c.102C>G	NP_003968.3:p.Ala34=
XM_024448761.1:c.102C>G	XP_024304529.1:p.Ala34=
NM_003977.4:c.102C>G MANE Select	NP_003968.3:p.Ala34=
NM_001302960.2:c.102C>G	NP_001289889.1:p.Ala34=
NM_001302959.2:c.-76C>G	NP_001289888.1:n.-76C>G