Canonical Allele Identifier: CA679490473

Gene: AIP

Linked Data

• dbSNP Id: rs1231587766
• MyVariant Identifiers: chr11:g.67250532A>G (hg19) ; chr11:g.67483061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483061A>G , CM000673.2:g.67483061A>G	GRCh38
NC_000011.9:g.67250532A>G , CM000673.1:g.67250532A>G	GRCh37
NC_000011.8:g.67007108A>G	NCBI36
NG_008969.1:g.5028A>G , LRG_460:g.5028A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.-98A>G	ENSP00000434982.3:n.-98A>G
ENST00000682699.1:c.-98A>G	ENSP00000507935.1:n.-98A>G
ENST00000279146.8:c.-98A>G MANE Select	ENSP00000279146.3:n.-98A>G
ENST00000279146.7:c.-98A>G	ENSP00000279146.3:n.-98A>G
ENST00000528641.6:c.-98A>G	ENSP00000434982.2:n.-98A>G
ENST00000529797.1:n.13A>G
NM_001302960.1:c.-98A>G	NP_001289889.1:n.-98A>G
NM_003977.3:c.-98A>G	NP_003968.3:n.-98A>G
XM_024448761.1:c.-98A>G	XP_024304529.1:n.-98A>G
NM_003977.4:c.-98A>G MANE Select	NP_003968.3:n.-98A>G
NM_001302960.2:c.-98A>G	NP_001289889.1:n.-98A>G