Canonical Allele Identifier: CA475509188

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257598C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490127C>T , CM000673.2:g.67490127C>T	GRCh38
NC_000011.9:g.67257598C>T , CM000673.1:g.67257598C>T	GRCh37
NC_000011.8:g.67014174C>T	NCBI36
NG_008969.1:g.12094C>T , LRG_460:g.12094C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.535C>T
ENST00000528641.7:c.369C>T	ENSP00000434982.3:p.Gly123=
ENST00000529797.2:n.1070C>T
ENST00000682324.1:c.468+672C>T	ENSP00000508017.1:n.468+672C>T
ENST00000682659.1:c.189C>T	ENSP00000507351.1:p.Gly63=
ENST00000682699.1:c.558C>T	ENSP00000507935.1:p.Gly186=
ENST00000683237.1:c.558C>T	ENSP00000507343.1:p.Gly186=
ENST00000683856.1:c.381C>T	ENSP00000507979.1:p.Gly127=
ENST00000684006.1:c.558C>T	ENSP00000507269.1:p.Gly186=
ENST00000684657.1:c.378C>T	ENSP00000507961.1:p.Gly126=
ENST00000279146.8:c.558C>T MANE Select	ENSP00000279146.3:p.Gly186=
ENST00000279146.7:c.558C>T	ENSP00000279146.3:p.Gly186=
ENST00000525341.1:c.210C>T	ENSP00000476993.1:p.Gly70=
ENST00000528641.6:c.369C>T	ENSP00000434982.2:p.Gly123=
NM_001302959.1:c.381C>T	NP_001289888.1:p.Gly127=
NM_001302960.1:c.558C>T	NP_001289889.1:p.Gly186=
NM_003977.3:c.558C>T	NP_003968.3:p.Gly186=
XM_024448761.1:c.558C>T	XP_024304529.1:p.Gly186=
NM_003977.4:c.558C>T MANE Select	NP_003968.3:p.Gly186=
NM_001302960.2:c.558C>T	NP_001289889.1:p.Gly186=
NM_001302959.2:c.381C>T	NP_001289888.1:p.Gly127=