Canonical Allele Identifier: CA2614621963

Gene: AIP

Linked Data

• gnomAD v4: 11-67489653-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489655del , CM000673.2:g.67489655del	GRCh38
NC_000011.9:g.67257126del , CM000673.1:g.67257126del	GRCh37
NC_000011.8:g.67013702del	NCBI36
NG_008969.1:g.11622del , LRG_460:g.11622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+200del
ENST00000528641.7:c.280-383del	ENSP00000434982.3:n.280-383del
ENST00000529797.2:n.598del
ENST00000682324.1:c.468+200del	ENSP00000508017.1:n.468+200del
ENST00000682659.1:c.100-383del	ENSP00000507351.1:n.100-383del
ENST00000682699.1:c.468+200del	ENSP00000507935.1:n.468+200del
ENST00000683237.1:c.468+200del	ENSP00000507343.1:n.468+200del
ENST00000683856.1:c.291+200del	ENSP00000507979.1:n.291+200del
ENST00000684006.1:c.468+200del	ENSP00000507269.1:n.468+200del
ENST00000684657.1:c.288+200del	ENSP00000507961.1:n.288+200del
ENST00000279146.8:c.468+200del MANE Select	ENSP00000279146.3:n.468+200del
ENST00000279146.7:c.468+200del	ENSP00000279146.3:n.468+200del
ENST00000525341.1:c.120+200del	ENSP00000476993.1:n.120+200del
ENST00000528641.6:c.280-383del	ENSP00000434982.2:n.280-383del
ENST00000529797.1:n.778del
NM_001302959.1:c.291+200del	NP_001289888.1:n.291+200del
NM_001302960.1:c.468+200del	NP_001289889.1:n.468+200del
NM_003977.3:c.468+200del	NP_003968.3:n.468+200del
XM_024448761.1:c.468+200del	XP_024304529.1:n.468+200del
NM_003977.4:c.468+200del MANE Select	NP_003968.3:n.468+200del
NM_001302960.2:c.468+200del	NP_001289889.1:n.468+200del
NM_001302959.2:c.291+200del	NP_001289888.1:n.291+200del