Canonical Allele Identifier: CA475509590

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258359A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490888A>C , CM000673.2:g.67490888A>C	GRCh38
NC_000011.9:g.67258359A>C , CM000673.1:g.67258359A>C	GRCh37
NC_000011.8:g.67014935A>C	NCBI36
NG_008969.1:g.12855A>C , LRG_460:g.12855A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1195A>C
ENST00000528641.7:c.699A>C	ENSP00000434982.3:p.Pro233=
ENST00000529797.2:n.1730A>C
ENST00000682324.1:c.469-109A>C	ENSP00000508017.1:n.469-109A>C
ENST00000682659.1:c.519A>C	ENSP00000507351.1:p.Pro173=
ENST00000682699.1:c.888A>C	ENSP00000507935.1:p.Pro296=
ENST00000683237.1:c.*28A>C	ENSP00000507343.1:n.*28A>C
ENST00000683856.1:c.711A>C	ENSP00000507979.1:p.Pro237=
ENST00000684006.1:c.*28A>C	ENSP00000507269.1:n.*28A>C
ENST00000684657.1:c.708A>C	ENSP00000507961.1:p.Pro236=
ENST00000279146.8:c.888A>C MANE Select	ENSP00000279146.3:p.Pro296=
ENST00000279146.7:c.888A>C	ENSP00000279146.3:p.Pro296=
NM_001302959.1:c.711A>C	NP_001289888.1:p.Pro237=
NM_001302960.1:c.*28A>C	NP_001289889.1:n.*28A>C
NM_003977.3:c.888A>C	NP_003968.3:p.Pro296=
XM_024448761.1:c.888A>C	XP_024304529.1:p.Pro296=
NM_003977.4:c.888A>C MANE Select	NP_003968.3:p.Pro296=
NM_001302960.2:c.*28A>C	NP_001289889.1:n.*28A>C
NM_001302959.2:c.711A>C	NP_001289888.1:p.Pro237=