Canonical Allele Identifier: CA475509744

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258440G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490969G>C , CM000673.2:g.67490969G>C	GRCh38
NC_000011.9:g.67258440G>C , CM000673.1:g.67258440G>C	GRCh37
NC_000011.8:g.67015016G>C	NCBI36
NG_008969.1:g.12936G>C , LRG_460:g.12936G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1276G>C
ENST00000528641.7:c.780G>C	ENSP00000434982.3:p.Arg260=
ENST00000529797.2:n.1811G>C
ENST00000682324.1:c.469-28G>C	ENSP00000508017.1:n.469-28G>C
ENST00000682659.1:c.600G>C	ENSP00000507351.1:p.Arg200=
ENST00000683237.1:c.*109G>C	ENSP00000507343.1:n.*109G>C
ENST00000683856.1:c.792G>C	ENSP00000507979.1:p.Arg264=
ENST00000684006.1:c.*109G>C	ENSP00000507269.1:n.*109G>C
ENST00000684657.1:c.789G>C	ENSP00000507961.1:p.Arg263=
ENST00000279146.8:c.969G>C MANE Select	ENSP00000279146.3:p.Arg323=
ENST00000279146.7:c.969G>C	ENSP00000279146.3:p.Arg323=
NM_001302959.1:c.792G>C	NP_001289888.1:p.Arg264=
NM_001302960.1:c.*109G>C	NP_001289889.1:n.*109G>C
NM_003977.3:c.969G>C	NP_003968.3:p.Arg323=
XM_024448761.1:c.969G>C	XP_024304529.1:p.Arg323=
NM_003977.4:c.969G>C MANE Select	NP_003968.3:p.Arg323=
NM_001302960.2:c.*109G>C	NP_001289889.1:n.*109G>C
NM_001302959.2:c.792G>C	NP_001289888.1:p.Arg264=