Canonical Allele Identifier: CA381555302

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258380C>A (hg19) ; chr11:g.67490909C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490909C>A , CM000673.2:g.67490909C>A	GRCh38
NC_000011.9:g.67258380C>A , CM000673.1:g.67258380C>A	GRCh37
NC_000011.8:g.67014956C>A	NCBI36
NG_008969.1:g.12876C>A , LRG_460:g.12876C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1216C>A
ENST00000528641.7:c.720C>A	ENSP00000434982.3:p.Ser240Arg
ENST00000529797.2:n.1751C>A
ENST00000682324.1:c.469-88C>A	ENSP00000508017.1:n.469-88C>A
ENST00000682659.1:c.540C>A	ENSP00000507351.1:p.Ser180Arg
ENST00000682699.1:c.909C>A	ENSP00000507935.1:p.Ser303Arg
ENST00000683237.1:c.*49C>A	ENSP00000507343.1:n.*49C>A
ENST00000683856.1:c.732C>A	ENSP00000507979.1:p.Ser244Arg
ENST00000684006.1:c.*49C>A	ENSP00000507269.1:n.*49C>A
ENST00000684657.1:c.729C>A	ENSP00000507961.1:p.Ser243Arg
ENST00000279146.8:c.909C>A MANE Select	ENSP00000279146.3:p.Ser303Arg
ENST00000279146.7:c.909C>A	ENSP00000279146.3:p.Ser303Arg
NM_001302959.1:c.732C>A	NP_001289888.1:p.Ser244Arg
NM_001302960.1:c.*49C>A	NP_001289889.1:n.*49C>A
NM_003977.3:c.909C>A	NP_003968.3:p.Ser303Arg
XM_024448761.1:c.909C>A	XP_024304529.1:p.Ser303Arg
NM_003977.4:c.909C>A MANE Select	NP_003968.3:p.Ser303Arg
NM_001302960.2:c.*49C>A	NP_001289889.1:n.*49C>A
NM_001302959.2:c.732C>A	NP_001289888.1:p.Ser244Arg