Canonical Allele Identifier: CA224164328

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489332G>C , CM000673.2:g.67489332G>C	GRCh38
NC_000011.9:g.67256803G>C , CM000673.1:g.67256803G>C	GRCh37
NC_000011.8:g.67013379G>C	NCBI36
NG_008969.1:g.11299G>C , LRG_460:g.11299G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.345G>C MANE Select	NP_003968.3:p.Leu115=
ENST00000279146.8:c.345G>C MANE Select	ENSP00000279146.3:p.Leu115=
NM_001302959.1:c.168G>C	NP_001289888.1:p.Leu56=
NM_001302959.2:c.168G>C	NP_001289888.1:p.Leu56=
NM_001302960.1:c.345G>C	NP_001289889.1:p.Leu115=
NM_001302960.2:c.345G>C	NP_001289889.1:p.Leu115=
NM_003977.3:c.345G>C	NP_003968.3:p.Leu115=
ENST00000279146.7:c.345G>C	ENSP00000279146.3:p.Leu115=
ENST00000525341.2:c.322G>C
ENST00000528641.6:c.280-706G>C	ENSP00000434982.2:n.280-706G>C
ENST00000528641.7:c.280-706G>C	ENSP00000434982.3:n.280-706G>C
ENST00000529797.1:n.455G>C
ENST00000529797.2:n.275G>C
ENST00000682324.1:c.345G>C	ENSP00000508017.1:p.Leu115=
ENST00000682659.1:c.100-706G>C	ENSP00000507351.1:n.100-706G>C
ENST00000682699.1:c.345G>C	ENSP00000507935.1:p.Leu115=
ENST00000683237.1:c.345G>C	ENSP00000507343.1:p.Leu115=
ENST00000683856.1:c.168G>C	ENSP00000507979.1:p.Leu56=
ENST00000684006.1:c.345G>C	ENSP00000507269.1:p.Leu115=
ENST00000684657.1:c.165G>C	ENSP00000507961.1:p.Leu55=
XM_024448761.1:c.345G>C	XP_024304529.1:p.Leu115=