Canonical Allele Identifier: CA2975261925

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490062_67490064del , CM000673.2:g.67490062_67490064del	GRCh38
NC_000011.9:g.67257533_67257535del , CM000673.1:g.67257533_67257535del	GRCh37
NC_000011.8:g.67014109_67014111del	NCBI36
NG_008969.1:g.12029_12031del , LRG_460:g.12029_12031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.470_472del
ENST00000528641.7:c.304_306del	ENSP00000434982.3:p.Gln102del
ENST00000529797.2:n.1005_1007del
ENST00000682324.1:c.468+607_468+609del	ENSP00000508017.1:n.468+607_468+609del
ENST00000682659.1:c.124_126del	ENSP00000507351.1:p.Gln42del
ENST00000682699.1:c.493_495del	ENSP00000507935.1:p.Gln165del
ENST00000683237.1:c.493_495del	ENSP00000507343.1:p.Gln165del
ENST00000683856.1:c.316_318del	ENSP00000507979.1:p.Gln106del
ENST00000684006.1:c.493_495del	ENSP00000507269.1:p.Gln165del
ENST00000684657.1:c.313_315del	ENSP00000507961.1:p.Gln105del
ENST00000279146.8:c.493_495del MANE Select	ENSP00000279146.3:p.Gln165del
ENST00000279146.7:c.493_495del	ENSP00000279146.3:p.Gln165del
ENST00000525341.1:c.145_147del	ENSP00000476993.1:p.Gln49del
ENST00000528641.6:c.304_306del	ENSP00000434982.2:p.Gln102del
NM_001302959.1:c.316_318del	NP_001289888.1:p.Gln106del
NM_001302960.1:c.493_495del	NP_001289889.1:p.Gln165del
NM_003977.3:c.493_495del	NP_003968.3:p.Gln165del
XM_024448761.1:c.493_495del	XP_024304529.1:p.Gln165del
NM_003977.4:c.493_495del MANE Select	NP_003968.3:p.Gln165del
NM_001302960.2:c.493_495del	NP_001289889.1:p.Gln165del
NM_001302959.2:c.316_318del	NP_001289888.1:p.Gln106del