Canonical Allele Identifier: CA381550462

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257543G>T (hg19) ; chr11:g.67490072G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490072G>T , CM000673.2:g.67490072G>T	GRCh38
NC_000011.9:g.67257543G>T , CM000673.1:g.67257543G>T	GRCh37
NC_000011.8:g.67014119G>T	NCBI36
NG_008969.1:g.12039G>T , LRG_460:g.12039G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.480G>T
ENST00000528641.7:c.314G>T	ENSP00000434982.3:p.Trp105Leu
ENST00000529797.2:n.1015G>T
ENST00000682324.1:c.468+617G>T	ENSP00000508017.1:n.468+617G>T
ENST00000682659.1:c.134G>T	ENSP00000507351.1:p.Trp45Leu
ENST00000682699.1:c.503G>T	ENSP00000507935.1:p.Trp168Leu
ENST00000683237.1:c.503G>T	ENSP00000507343.1:p.Trp168Leu
ENST00000683856.1:c.326G>T	ENSP00000507979.1:p.Trp109Leu
ENST00000684006.1:c.503G>T	ENSP00000507269.1:p.Trp168Leu
ENST00000684657.1:c.323G>T	ENSP00000507961.1:p.Trp108Leu
ENST00000279146.8:c.503G>T MANE Select	ENSP00000279146.3:p.Trp168Leu
ENST00000279146.7:c.503G>T	ENSP00000279146.3:p.Trp168Leu
ENST00000525341.1:c.155G>T	ENSP00000476993.1:p.Trp52Leu
ENST00000528641.6:c.314G>T	ENSP00000434982.2:p.Trp105Leu
NM_001302959.1:c.326G>T	NP_001289888.1:p.Trp109Leu
NM_001302960.1:c.503G>T	NP_001289889.1:p.Trp168Leu
NM_003977.3:c.503G>T	NP_003968.3:p.Trp168Leu
XM_024448761.1:c.503G>T	XP_024304529.1:p.Trp168Leu
NM_003977.4:c.503G>T MANE Select	NP_003968.3:p.Trp168Leu
NM_001302960.2:c.503G>T	NP_001289889.1:p.Trp168Leu
NM_001302959.2:c.326G>T	NP_001289888.1:p.Trp109Leu