Canonical Allele Identifier: CA381554318

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258265T>C (hg19) ; chr11:g.67490794T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490794T>C , CM000673.2:g.67490794T>C	GRCh38
NC_000011.9:g.67258265T>C , CM000673.1:g.67258265T>C	GRCh37
NC_000011.8:g.67014841T>C	NCBI36
NG_008969.1:g.12761T>C , LRG_460:g.12761T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1101T>C
ENST00000528641.7:c.605T>C	ENSP00000434982.3:p.Val202Ala
ENST00000529797.2:n.1636T>C
ENST00000682324.1:c.469-203T>C	ENSP00000508017.1:n.469-203T>C
ENST00000682659.1:c.425T>C	ENSP00000507351.1:p.Val142Ala
ENST00000682699.1:c.794T>C	ENSP00000507935.1:p.Val265Ala
ENST00000683237.1:c.786T>C	ENSP00000507343.1:p.Arg262=
ENST00000683856.1:c.617T>C	ENSP00000507979.1:p.Val206Ala
ENST00000684006.1:c.788-5T>C	ENSP00000507269.1:n.788-5T>C
ENST00000684657.1:c.614T>C	ENSP00000507961.1:p.Val205Ala
ENST00000279146.8:c.794T>C MANE Select	ENSP00000279146.3:p.Val265Ala
ENST00000279146.7:c.794T>C	ENSP00000279146.3:p.Val265Ala
ENST00000528641.6:c.605T>C	ENSP00000434982.2:p.Val202Ala
NM_001302959.1:c.617T>C	NP_001289888.1:p.Val206Ala
NM_001302960.1:c.786T>C	NP_001289889.1:p.Arg262=
NM_003977.3:c.794T>C	NP_003968.3:p.Val265Ala
XM_024448761.1:c.794T>C	XP_024304529.1:p.Val265Ala
NM_003977.4:c.794T>C MANE Select	NP_003968.3:p.Val265Ala
NM_001302960.2:c.786T>C	NP_001289889.1:p.Arg262=
NM_001302959.2:c.617T>C	NP_001289888.1:p.Val206Ala