Canonical Allele Identifier: CA679490460

Gene: AIP

Linked Data

• dbSNP Id: rs1273056692
• MyVariant Identifiers: chr11:g.67250497_67250518del (hg19) ; chr11:g.67483026_67483047del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483028_67483049del , CM000673.2:g.67483028_67483049del	GRCh38
NC_000011.9:g.67250499_67250520del , CM000673.1:g.67250499_67250520del	GRCh37
NC_000011.8:g.67007075_67007096del	NCBI36
NG_008969.1:g.4995_5016del , LRG_460:g.4995_5016del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682699.1:c.-131_-110del	ENSP00000507935.1:n.-131_-110del
ENST00000279146.8:c.-131_-110del MANE Select	ENSP00000279146.3:n.-131_-110del
XM_024448761.1:c.-131_-110del	XP_024304529.1:n.-131_-110del
NM_003977.4:c.-131_-110del MANE Select	NP_003968.3:n.-131_-110del
NM_001302960.2:c.-131_-110del	NP_001289889.1:n.-131_-110del