Canonical Allele Identifier: CA381551963

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257930T>A (hg19) ; chr11:g.67490459T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490459T>A , CM000673.2:g.67490459T>A	GRCh38
NC_000011.9:g.67257930T>A , CM000673.1:g.67257930T>A	GRCh37
NC_000011.8:g.67014506T>A	NCBI36
NG_008969.1:g.12426T>A , LRG_460:g.12426T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.766T>A
ENST00000528641.7:c.598+2T>A	ENSP00000434982.3:n.598+2T>A
ENST00000529797.2:n.1301T>A
ENST00000682324.1:c.469-538T>A	ENSP00000508017.1:n.469-538T>A
ENST00000682659.1:c.418+2T>A	ENSP00000507351.1:n.418+2T>A
ENST00000682699.1:c.787+2T>A	ENSP00000507935.1:n.787+2T>A
ENST00000683237.1:c.779+10T>A	ENSP00000507343.1:n.779+10T>A
ENST00000683856.1:c.610+2T>A	ENSP00000507979.1:n.610+2T>A
ENST00000684006.1:c.787+2T>A	ENSP00000507269.1:n.787+2T>A
ENST00000684657.1:c.607+2T>A	ENSP00000507961.1:n.607+2T>A
ENST00000279146.8:c.787+2T>A MANE Select	ENSP00000279146.3:n.787+2T>A
ENST00000279146.7:c.787+2T>A	ENSP00000279146.3:n.787+2T>A
ENST00000525341.1:c.441T>A	ENSP00000476993.1:p.Gly147=
ENST00000528641.6:c.598+2T>A	ENSP00000434982.2:n.598+2T>A
NM_001302959.1:c.610+2T>A	NP_001289888.1:n.610+2T>A
NM_001302960.1:c.779+10T>A	NP_001289889.1:n.779+10T>A
NM_003977.3:c.787+2T>A	NP_003968.3:n.787+2T>A
XM_024448761.1:c.787+2T>A	XP_024304529.1:n.787+2T>A
NM_003977.4:c.787+2T>A MANE Select	NP_003968.3:n.787+2T>A
NM_001302960.2:c.779+10T>A	NP_001289889.1:n.779+10T>A
NM_001302959.2:c.610+2T>A	NP_001289888.1:n.610+2T>A