Canonical Allele Identifier: CA599911431

Gene: AIP

Linked Data

• dbSNP Id: rs1405408726
• gnomAD v2: 11-67257159-TTC-T
• gnomAD v4: 11-67489688-TTC-T
• MyVariant Identifiers: chr11:g.67257160_67257161del (hg19) ; chr11:g.67489689_67489690del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489692_67489693del , CM000673.2:g.67489692_67489693del	GRCh38
NC_000011.9:g.67257163_67257164del , CM000673.1:g.67257163_67257164del	GRCh37
NC_000011.8:g.67013739_67013740del	NCBI36
NG_008969.1:g.11659_11660del , LRG_460:g.11659_11660del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+237_445+238del
ENST00000528641.7:c.280-346_280-345del	ENSP00000434982.3:n.280-346_280-345del
ENST00000529797.2:n.635_636del
ENST00000682324.1:c.468+237_468+238del	ENSP00000508017.1:n.468+237_468+238del
ENST00000682659.1:c.100-346_100-345del	ENSP00000507351.1:n.100-346_100-345del
ENST00000682699.1:c.468+237_468+238del	ENSP00000507935.1:n.468+237_468+238del
ENST00000683237.1:c.468+237_468+238del	ENSP00000507343.1:n.468+237_468+238del
ENST00000683856.1:c.291+237_291+238del	ENSP00000507979.1:n.291+237_291+238del
ENST00000684006.1:c.468+237_468+238del	ENSP00000507269.1:n.468+237_468+238del
ENST00000684657.1:c.288+237_288+238del	ENSP00000507961.1:n.288+237_288+238del
ENST00000279146.8:c.468+237_468+238del MANE Select	ENSP00000279146.3:n.468+237_468+238del
ENST00000279146.7:c.468+237_468+238del	ENSP00000279146.3:n.468+237_468+238del
ENST00000525341.1:c.120+237_120+238del	ENSP00000476993.1:n.120+237_120+238del
ENST00000528641.6:c.280-346_280-345del	ENSP00000434982.2:n.280-346_280-345del
NM_001302959.1:c.291+237_291+238del	NP_001289888.1:n.291+237_291+238del
NM_001302960.1:c.468+237_468+238del	NP_001289889.1:n.468+237_468+238del
NM_003977.3:c.468+237_468+238del	NP_003968.3:n.468+237_468+238del
XM_024448761.1:c.468+237_468+238del	XP_024304529.1:n.468+237_468+238del
NM_003977.4:c.468+237_468+238del MANE Select	NP_003968.3:n.468+237_468+238del
NM_001302960.2:c.468+237_468+238del	NP_001289889.1:n.468+237_468+238del
NM_001302959.2:c.291+237_291+238del	NP_001289888.1:n.291+237_291+238del