Canonical Allele Identifier: CA381551491

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257799T>A (hg19) ; chr11:g.67490328T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490328T>A , CM000673.2:g.67490328T>A	GRCh38
NC_000011.9:g.67257799T>A , CM000673.1:g.67257799T>A	GRCh37
NC_000011.8:g.67014375T>A	NCBI36
NG_008969.1:g.12295T>A , LRG_460:g.12295T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.635T>A
ENST00000528641.7:c.469T>A	ENSP00000434982.3:p.Ser157Thr
ENST00000529797.2:n.1170T>A
ENST00000682324.1:c.469-669T>A	ENSP00000508017.1:n.469-669T>A
ENST00000682659.1:c.289T>A	ENSP00000507351.1:p.Ser97Thr
ENST00000682699.1:c.658T>A	ENSP00000507935.1:p.Ser220Thr
ENST00000683237.1:c.658T>A	ENSP00000507343.1:p.Ser220Thr
ENST00000683856.1:c.481T>A	ENSP00000507979.1:p.Ser161Thr
ENST00000684006.1:c.658T>A	ENSP00000507269.1:p.Ser220Thr
ENST00000684657.1:c.478T>A	ENSP00000507961.1:p.Ser160Thr
ENST00000279146.8:c.658T>A MANE Select	ENSP00000279146.3:p.Ser220Thr
ENST00000279146.7:c.658T>A	ENSP00000279146.3:p.Ser220Thr
ENST00000525341.1:c.310T>A	ENSP00000476993.1:p.Ser104Thr
ENST00000528641.6:c.469T>A	ENSP00000434982.2:p.Ser157Thr
NM_001302959.1:c.481T>A	NP_001289888.1:p.Ser161Thr
NM_001302960.1:c.658T>A	NP_001289889.1:p.Ser220Thr
NM_003977.3:c.658T>A	NP_003968.3:p.Ser220Thr
XM_024448761.1:c.658T>A	XP_024304529.1:p.Ser220Thr
NM_003977.4:c.658T>A MANE Select	NP_003968.3:p.Ser220Thr
NM_001302960.2:c.658T>A	NP_001289889.1:p.Ser220Thr
NM_001302959.2:c.481T>A	NP_001289888.1:p.Ser161Thr