Canonical Allele Identifier: CA918903878

Gene: AIP

Linked Data

• dbSNP Id: rs1565180257

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483056_67483058del , CM000673.2:g.67483056_67483058del	GRCh38
NC_000011.9:g.67250527_67250529del , CM000673.1:g.67250527_67250529del	GRCh37
NC_000011.8:g.67007103_67007105del	NCBI36
NG_008969.1:g.5023_5025del , LRG_460:g.5023_5025del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.-103_-101del	ENSP00000434982.3:n.-103_-101del
ENST00000682699.1:c.-103_-101del	ENSP00000507935.1:n.-103_-101del
ENST00000279146.8:c.-103_-101del MANE Select	ENSP00000279146.3:n.-103_-101del
ENST00000279146.7:c.-103_-101del	ENSP00000279146.3:n.-103_-101del
ENST00000528641.6:c.-103_-101del	ENSP00000434982.2:n.-103_-101del
ENST00000529797.1:n.8_10del
NM_001302960.1:c.-103_-101del	NP_001289889.1:n.-103_-101del
NM_003977.3:c.-103_-101del	NP_003968.3:n.-103_-101del
XM_024448761.1:c.-103_-101del	XP_024304529.1:n.-103_-101del
NM_003977.4:c.-103_-101del MANE Select	NP_003968.3:n.-103_-101del
NM_001302960.2:c.-103_-101del	NP_001289889.1:n.-103_-101del