Canonical Allele Identifier: CA475509155

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257553A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490082A>T , CM000673.2:g.67490082A>T	GRCh38
NC_000011.9:g.67257553A>T , CM000673.1:g.67257553A>T	GRCh37
NC_000011.8:g.67014129A>T	NCBI36
NG_008969.1:g.12049A>T , LRG_460:g.12049A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.490A>T
ENST00000528641.7:c.324A>T	ENSP00000434982.3:p.Thr108=
ENST00000529797.2:n.1025A>T
ENST00000682324.1:c.468+627A>T	ENSP00000508017.1:n.468+627A>T
ENST00000682659.1:c.144A>T	ENSP00000507351.1:p.Thr48=
ENST00000682699.1:c.513A>T	ENSP00000507935.1:p.Thr171=
ENST00000683237.1:c.513A>T	ENSP00000507343.1:p.Thr171=
ENST00000683856.1:c.336A>T	ENSP00000507979.1:p.Thr112=
ENST00000684006.1:c.513A>T	ENSP00000507269.1:p.Thr171=
ENST00000684657.1:c.333A>T	ENSP00000507961.1:p.Thr111=
ENST00000279146.8:c.513A>T MANE Select	ENSP00000279146.3:p.Thr171=
ENST00000279146.7:c.513A>T	ENSP00000279146.3:p.Thr171=
ENST00000525341.1:c.165A>T	ENSP00000476993.1:p.Thr55=
ENST00000528641.6:c.324A>T	ENSP00000434982.2:p.Thr108=
NM_001302959.1:c.336A>T	NP_001289888.1:p.Thr112=
NM_001302960.1:c.513A>T	NP_001289889.1:p.Thr171=
NM_003977.3:c.513A>T	NP_003968.3:p.Thr171=
XM_024448761.1:c.513A>T	XP_024304529.1:p.Thr171=
NM_003977.4:c.513A>T MANE Select	NP_003968.3:p.Thr171=
NM_001302960.2:c.513A>T	NP_001289889.1:p.Thr171=
NM_001302959.2:c.336A>T	NP_001289888.1:p.Thr112=