Canonical Allele Identifier: CA475509558

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258344G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490873G>T , CM000673.2:g.67490873G>T	GRCh38
NC_000011.9:g.67258344G>T , CM000673.1:g.67258344G>T	GRCh37
NC_000011.8:g.67014920G>T	NCBI36
NG_008969.1:g.12840G>T , LRG_460:g.12840G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1180G>T
ENST00000528641.7:c.684G>T	ENSP00000434982.3:p.Val228=
ENST00000529797.2:n.1715G>T
ENST00000682324.1:c.469-124G>T	ENSP00000508017.1:n.469-124G>T
ENST00000682659.1:c.504G>T	ENSP00000507351.1:p.Val168=
ENST00000682699.1:c.873G>T	ENSP00000507935.1:p.Val291=
ENST00000683237.1:c.*13G>T	ENSP00000507343.1:n.*13G>T
ENST00000683856.1:c.696G>T	ENSP00000507979.1:p.Val232=
ENST00000684006.1:c.*13G>T	ENSP00000507269.1:n.*13G>T
ENST00000684657.1:c.693G>T	ENSP00000507961.1:p.Val231=
ENST00000279146.8:c.873G>T MANE Select	ENSP00000279146.3:p.Val291=
ENST00000279146.7:c.873G>T	ENSP00000279146.3:p.Val291=
ENST00000528641.6:c.684G>T	ENSP00000434982.2:p.Val228=
NM_001302959.1:c.696G>T	NP_001289888.1:p.Val232=
NM_001302960.1:c.*13G>T	NP_001289889.1:n.*13G>T
NM_003977.3:c.873G>T	NP_003968.3:p.Val291=
XM_024448761.1:c.873G>T	XP_024304529.1:p.Val291=
NM_003977.4:c.873G>T MANE Select	NP_003968.3:p.Val291=
NM_001302960.2:c.*13G>T	NP_001289889.1:n.*13G>T
NM_001302959.2:c.696G>T	NP_001289888.1:p.Val232=