Canonical Allele Identifier: CA6140970

Gene: AIP

Linked Data

• dbSNP Id: rs376695792
• ExAC: 11:67258210 T / TC
• gnomAD v2: 11-67258210-T-TC
• gnomAD v4: 11-67490739-T-TC
• MyVariant Identifiers: chr11:g.67258212_67258213insC (hg19) ; chr11:g.67258211_67258212insC (hg19) ; chr11:g.67258210_67258211insC (hg19) ; chr11:g.67490739_67490740insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490745dup , CM000673.2:g.67490745dup	GRCh38
NC_000011.9:g.67258216dup , CM000673.1:g.67258216dup	GRCh37
NC_000011.8:g.67014792dup	NCBI36
NG_008969.1:g.12712dup , LRG_460:g.12712dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1052dup
ENST00000528641.7:c.599-43dup	ENSP00000434982.3:n.599-43dup
ENST00000529797.2:n.1587dup
ENST00000682324.1:c.469-252dup	ENSP00000508017.1:n.469-252dup
ENST00000682659.1:c.419-43dup	ENSP00000507351.1:n.419-43dup
ENST00000682699.1:c.788-43dup	ENSP00000507935.1:n.788-43dup
ENST00000683237.1:c.780-43dup	ENSP00000507343.1:n.780-43dup
ENST00000683856.1:c.611-43dup	ENSP00000507979.1:n.611-43dup
ENST00000684006.1:c.788-54dup	ENSP00000507269.1:n.788-54dup
ENST00000684657.1:c.608-43dup	ENSP00000507961.1:n.608-43dup
ENST00000279146.8:c.788-43dup MANE Select	ENSP00000279146.3:n.788-43dup
ENST00000279146.7:c.788-43dup	ENSP00000279146.3:n.788-43dup
ENST00000528641.6:c.599-43dup	ENSP00000434982.2:n.599-43dup
NM_001302959.1:c.611-43dup	NP_001289888.1:n.611-43dup
NM_001302960.1:c.780-43dup	NP_001289889.1:n.780-43dup
NM_003977.3:c.788-43dup	NP_003968.3:n.788-43dup
XM_024448761.1:c.788-43dup	XP_024304529.1:n.788-43dup
NM_003977.4:c.788-43dup MANE Select	NP_003968.3:n.788-43dup
NM_001302960.2:c.780-43dup	NP_001289889.1:n.780-43dup
NM_001302959.2:c.611-43dup	NP_001289888.1:n.611-43dup