Canonical Allele Identifier: CA381549087

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67256789G>C (hg19) ; chr11:g.67489318G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489318G>C , CM000673.2:g.67489318G>C	GRCh38
NC_000011.9:g.67256789G>C , CM000673.1:g.67256789G>C	GRCh37
NC_000011.8:g.67013365G>C	NCBI36
NG_008969.1:g.11285G>C , LRG_460:g.11285G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.308G>C
ENST00000528641.7:c.280-720G>C	ENSP00000434982.3:n.280-720G>C
ENST00000529797.2:n.261G>C
ENST00000682324.1:c.331G>C	ENSP00000508017.1:p.Gly111Arg
ENST00000682659.1:c.100-720G>C	ENSP00000507351.1:n.100-720G>C
ENST00000682699.1:c.331G>C	ENSP00000507935.1:p.Gly111Arg
ENST00000683237.1:c.331G>C	ENSP00000507343.1:p.Gly111Arg
ENST00000683856.1:c.154G>C	ENSP00000507979.1:p.Gly52Arg
ENST00000684006.1:c.331G>C	ENSP00000507269.1:p.Gly111Arg
ENST00000684657.1:c.151G>C	ENSP00000507961.1:p.Gly51Arg
ENST00000279146.8:c.331G>C MANE Select	ENSP00000279146.3:p.Gly111Arg
ENST00000279146.7:c.331G>C	ENSP00000279146.3:p.Gly111Arg
ENST00000528641.6:c.280-720G>C	ENSP00000434982.2:n.280-720G>C
ENST00000529797.1:n.441G>C
NM_001302959.1:c.154G>C	NP_001289888.1:p.Gly52Arg
NM_001302960.1:c.331G>C	NP_001289889.1:p.Gly111Arg
NM_003977.3:c.331G>C	NP_003968.3:p.Gly111Arg
XM_024448761.1:c.331G>C	XP_024304529.1:p.Gly111Arg
NM_003977.4:c.331G>C MANE Select	NP_003968.3:p.Gly111Arg
NM_001302960.2:c.331G>C	NP_001289889.1:p.Gly111Arg
NM_001302959.2:c.154G>C	NP_001289888.1:p.Gly52Arg