Canonical Allele Identifier: CA381554729

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258311T>G (hg19) ; chr11:g.67490840T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490840T>G , CM000673.2:g.67490840T>G	GRCh38
NC_000011.9:g.67258311T>G , CM000673.1:g.67258311T>G	GRCh37
NC_000011.8:g.67014887T>G	NCBI36
NG_008969.1:g.12807T>G , LRG_460:g.12807T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1147T>G
ENST00000528641.7:c.651T>G	ENSP00000434982.3:p.Asn217Lys
ENST00000529797.2:n.1682T>G
ENST00000682324.1:c.469-157T>G	ENSP00000508017.1:n.469-157T>G
ENST00000682659.1:c.471T>G	ENSP00000507351.1:p.Asn157Lys
ENST00000682699.1:c.840T>G	ENSP00000507935.1:p.Asn280Lys
ENST00000683237.1:c.832T>G	ENSP00000507343.1:p.Cys278Gly
ENST00000683856.1:c.663T>G	ENSP00000507979.1:p.Asn221Lys
ENST00000684006.1:c.829T>G	ENSP00000507269.1:p.Cys277Gly
ENST00000684657.1:c.660T>G	ENSP00000507961.1:p.Asn220Lys
ENST00000279146.8:c.840T>G MANE Select	ENSP00000279146.3:p.Asn280Lys
ENST00000279146.7:c.840T>G	ENSP00000279146.3:p.Asn280Lys
ENST00000528641.6:c.651T>G	ENSP00000434982.2:p.Asn217Lys
NM_001302959.1:c.663T>G	NP_001289888.1:p.Asn221Lys
NM_001302960.1:c.832T>G	NP_001289889.1:p.Cys278Gly
NM_003977.3:c.840T>G	NP_003968.3:p.Asn280Lys
XM_024448761.1:c.840T>G	XP_024304529.1:p.Asn280Lys
NM_003977.4:c.840T>G MANE Select	NP_003968.3:p.Asn280Lys
NM_001302960.2:c.832T>G	NP_001289889.1:p.Cys278Gly
NM_001302959.2:c.663T>G	NP_001289888.1:p.Asn221Lys