Canonical Allele Identifier: CA475509579

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258353G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490882G>T , CM000673.2:g.67490882G>T	GRCh38
NC_000011.9:g.67258353G>T , CM000673.1:g.67258353G>T	GRCh37
NC_000011.8:g.67014929G>T	NCBI36
NG_008969.1:g.12849G>T , LRG_460:g.12849G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1189G>T
ENST00000528641.7:c.693G>T	ENSP00000434982.3:p.Leu231=
ENST00000529797.2:n.1724G>T
ENST00000682324.1:c.469-115G>T	ENSP00000508017.1:n.469-115G>T
ENST00000682659.1:c.513G>T	ENSP00000507351.1:p.Leu171=
ENST00000682699.1:c.882G>T	ENSP00000507935.1:p.Leu294=
ENST00000683237.1:c.*22G>T	ENSP00000507343.1:n.*22G>T
ENST00000683856.1:c.705G>T	ENSP00000507979.1:p.Leu235=
ENST00000684006.1:c.*22G>T	ENSP00000507269.1:n.*22G>T
ENST00000684657.1:c.702G>T	ENSP00000507961.1:p.Leu234=
ENST00000279146.8:c.882G>T MANE Select	ENSP00000279146.3:p.Leu294=
ENST00000279146.7:c.882G>T	ENSP00000279146.3:p.Leu294=
ENST00000528641.6:c.693G>T	ENSP00000434982.2:p.Leu231=
NM_001302959.1:c.705G>T	NP_001289888.1:p.Leu235=
NM_001302960.1:c.*22G>T	NP_001289889.1:n.*22G>T
NM_003977.3:c.882G>T	NP_003968.3:p.Leu294=
XM_024448761.1:c.882G>T	XP_024304529.1:p.Leu294=
NM_003977.4:c.882G>T MANE Select	NP_003968.3:p.Leu294=
NM_001302960.2:c.*22G>T	NP_001289889.1:n.*22G>T
NM_001302959.2:c.705G>T	NP_001289888.1:p.Leu235=