Canonical Allele Identifier: CA2792512322

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490216_67490316del , CM000673.2:g.67490216_67490316del	GRCh38
NC_000011.9:g.67257687_67257787del , CM000673.1:g.67257687_67257787del	GRCh37
NC_000011.8:g.67014263_67014363del	NCBI36
NG_008969.1:g.12183_12283del , LRG_460:g.12183_12283del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.622+2_623del
ENST00000528641.7:c.456+2_457del
ENST00000529797.2:n.1157+2_1158del
ENST00000682324.1:c.468+761_469-681del	ENSP00000508017.1:n.468+761_469-681del
ENST00000682659.1:c.276+2_277del
ENST00000682699.1:c.645+2_646del
ENST00000683237.1:c.645+2_646del
ENST00000683856.1:c.468+2_469del
ENST00000684006.1:c.645+2_646del
ENST00000684657.1:c.465+2_466del
ENST00000279146.8:c.645+2_646del
ENST00000279146.7:c.645+2_646del
ENST00000525341.1:c.297+2_298del
ENST00000528641.6:c.456+2_457del
NM_001302959.1:c.468+2_469del
NM_001302960.1:c.645+2_646del
NM_003977.3:c.645+2_646del
XM_024448761.1:c.645+2_646del
NM_003977.4:c.645+2_646del
NM_001302960.2:c.645+2_646del
NM_001302959.2:c.468+2_469del