Canonical Allele Identifier: CA475392243

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67254494G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487023G>T , CM000673.2:g.67487023G>T	GRCh38
NC_000011.9:g.67254494G>T , CM000673.1:g.67254494G>T	GRCh37
NC_000011.8:g.67011070G>T	NCBI36
NG_008969.1:g.8990G>T , LRG_460:g.8990G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.94G>T
ENST00000528641.7:c.117G>T	ENSP00000434982.3:p.Arg39=
ENST00000529797.2:n.47G>T
ENST00000682324.1:c.117G>T	ENSP00000508017.1:p.Arg39=
ENST00000682659.1:c.100-3015G>T	ENSP00000507351.1:n.100-3015G>T
ENST00000682699.1:c.117G>T	ENSP00000507935.1:p.Arg39=
ENST00000683237.1:c.117G>T	ENSP00000507343.1:p.Arg39=
ENST00000683856.1:c.-61G>T	ENSP00000507979.1:n.-61G>T
ENST00000684006.1:c.117G>T	ENSP00000507269.1:p.Arg39=
ENST00000684657.1:c.100-2244G>T	ENSP00000507961.1:n.100-2244G>T
ENST00000279146.8:c.117G>T MANE Select	ENSP00000279146.3:p.Arg39=
ENST00000279146.7:c.117G>T	ENSP00000279146.3:p.Arg39=
ENST00000528641.6:c.117G>T	ENSP00000434982.2:p.Arg39=
ENST00000529797.1:n.227G>T
NM_001302959.1:c.-61G>T	NP_001289888.1:n.-61G>T
NM_001302960.1:c.117G>T	NP_001289889.1:p.Arg39=
NM_003977.3:c.117G>T	NP_003968.3:p.Arg39=
XM_024448761.1:c.117G>T	XP_024304529.1:p.Arg39=
NM_003977.4:c.117G>T MANE Select	NP_003968.3:p.Arg39=
NM_001302960.2:c.117G>T	NP_001289889.1:p.Arg39=
NM_001302959.2:c.-61G>T	NP_001289888.1:n.-61G>T