Canonical Allele Identifier: CA1980172470

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490451_67490454delinsTACG , CM000673.2:g.67490451_67490454delinsTACG	GRCh38
NC_000011.9:g.67257922_67257925delinsTACG , CM000673.1:g.67257922_67257925delinsTACG	GRCh37
NC_000011.8:g.67014498_67014501delinsTACG	NCBI36
NG_008969.1:g.12418_12421delinsTACG , LRG_460:g.12418_12421delinsTACG

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.758_761delinsTACG
ENST00000528641.7:c.592_595delinsTACG	ENSP00000434982.3:p.Tyr198=
ENST00000529797.2:n.1293_1296delinsTACG
ENST00000682324.1:c.469-546_469-543delinsTACG	ENSP00000508017.1:n.469-546_469-543delins...
ENST00000682659.1:c.412_415delinsTACG	ENSP00000507351.1:p.Tyr138=
ENST00000682699.1:c.781_784delinsTACG	ENSP00000507935.1:p.Tyr261=
ENST00000683237.1:c.779+2_779+5delinsTACG	ENSP00000507343.1:n.779+2_779+5delinsTACG...
ENST00000683856.1:c.604_607delinsTACG	ENSP00000507979.1:p.Tyr202=
ENST00000684006.1:c.781_784delinsTACG	ENSP00000507269.1:p.Tyr261=
ENST00000684657.1:c.601_604delinsTACG	ENSP00000507961.1:p.Tyr201=
ENST00000279146.8:c.781_784delinsTACG MANE Select	ENSP00000279146.3:p.Tyr261=
ENST00000279146.7:c.781_784delinsTACG	ENSP00000279146.3:p.Tyr261=
ENST00000525341.1:c.433_436delinsTACG	ENSP00000476993.1:p.Tyr145=
ENST00000528641.6:c.592_595delinsTACG	ENSP00000434982.2:p.Tyr198=
NM_001302959.1:c.604_607delinsTACG	NP_001289888.1:p.Tyr202=
NM_001302960.1:c.779+2_779+5delinsTACG	NP_001289889.1:n.779+2_779+5delinsTACG
NM_003977.3:c.781_784delinsTACG	NP_003968.3:p.Tyr261=
XM_024448761.1:c.781_784delinsTACG	XP_024304529.1:p.Tyr261=
NM_003977.4:c.781_784delinsTACG MANE Select	NP_003968.3:p.Tyr261=
NM_001302960.2:c.779+2_779+5delinsTACG	NP_001289889.1:n.779+2_779+5delinsTACG
NM_001302959.2:c.604_607delinsTACG	NP_001289888.1:p.Tyr202=