Canonical Allele Identifier: CA381551585

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257824A>G (hg19) ; chr11:g.67490353A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490353A>G , CM000673.2:g.67490353A>G	GRCh38
NC_000011.9:g.67257824A>G , CM000673.1:g.67257824A>G	GRCh37
NC_000011.8:g.67014400A>G	NCBI36
NG_008969.1:g.12320A>G , LRG_460:g.12320A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.660A>G
ENST00000528641.7:c.494A>G	ENSP00000434982.3:p.Gln165Arg
ENST00000529797.2:n.1195A>G
ENST00000682324.1:c.469-644A>G	ENSP00000508017.1:n.469-644A>G
ENST00000682659.1:c.314A>G	ENSP00000507351.1:p.Gln105Arg
ENST00000682699.1:c.683A>G	ENSP00000507935.1:p.Gln228Arg
ENST00000683237.1:c.683A>G	ENSP00000507343.1:p.Gln228Arg
ENST00000683856.1:c.506A>G	ENSP00000507979.1:p.Gln169Arg
ENST00000684006.1:c.683A>G	ENSP00000507269.1:p.Gln228Arg
ENST00000684657.1:c.503A>G	ENSP00000507961.1:p.Gln168Arg
ENST00000279146.8:c.683A>G MANE Select	ENSP00000279146.3:p.Gln228Arg
ENST00000279146.7:c.683A>G	ENSP00000279146.3:p.Gln228Arg
ENST00000525341.1:c.335A>G	ENSP00000476993.1:p.Gln112Arg
ENST00000528641.6:c.494A>G	ENSP00000434982.2:p.Gln165Arg
NM_001302959.1:c.506A>G	NP_001289888.1:p.Gln169Arg
NM_001302960.1:c.683A>G	NP_001289889.1:p.Gln228Arg
NM_003977.3:c.683A>G	NP_003968.3:p.Gln228Arg
XM_024448761.1:c.683A>G	XP_024304529.1:p.Gln228Arg
NM_003977.4:c.683A>G MANE Select	NP_003968.3:p.Gln228Arg
NM_001302960.2:c.683A>G	NP_001289889.1:p.Gln228Arg
NM_001302959.2:c.506A>G	NP_001289888.1:p.Gln169Arg