Canonical Allele Identifier: CA381554492

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258288A>C (hg19) ; chr11:g.67490817A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490817A>C , CM000673.2:g.67490817A>C	GRCh38
NC_000011.9:g.67258288A>C , CM000673.1:g.67258288A>C	GRCh37
NC_000011.8:g.67014864A>C	NCBI36
NG_008969.1:g.12784A>C , LRG_460:g.12784A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1124A>C
ENST00000528641.7:c.628A>C	ENSP00000434982.3:p.Lys210Gln
ENST00000529797.2:n.1659A>C
ENST00000682324.1:c.469-180A>C	ENSP00000508017.1:n.469-180A>C
ENST00000682659.1:c.448A>C	ENSP00000507351.1:p.Lys150Gln
ENST00000682699.1:c.817A>C	ENSP00000507935.1:p.Lys273Gln
ENST00000683237.1:c.809A>C	ENSP00000507343.1:p.Gln270Pro
ENST00000683856.1:c.640A>C	ENSP00000507979.1:p.Lys214Gln
ENST00000684006.1:c.806A>C	ENSP00000507269.1:p.Gln269Pro
ENST00000684657.1:c.637A>C	ENSP00000507961.1:p.Lys213Gln
ENST00000279146.8:c.817A>C MANE Select	ENSP00000279146.3:p.Lys273Gln
ENST00000279146.7:c.817A>C	ENSP00000279146.3:p.Lys273Gln
ENST00000528641.6:c.628A>C	ENSP00000434982.2:p.Lys210Gln
NM_001302959.1:c.640A>C	NP_001289888.1:p.Lys214Gln
NM_001302960.1:c.809A>C	NP_001289889.1:p.Gln270Pro
NM_003977.3:c.817A>C	NP_003968.3:p.Lys273Gln
XM_024448761.1:c.817A>C	XP_024304529.1:p.Lys273Gln
NM_003977.4:c.817A>C MANE Select	NP_003968.3:p.Lys273Gln
NM_001302960.2:c.809A>C	NP_001289889.1:p.Gln270Pro
NM_001302959.2:c.640A>C	NP_001289888.1:p.Lys214Gln