Canonical Allele Identifier: CA2614622813

Gene: AIP

Linked Data

• gnomAD v4: 11-67489976-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489977del , CM000673.2:g.67489977del	GRCh38
NC_000011.9:g.67257448del , CM000673.1:g.67257448del	GRCh37
NC_000011.8:g.67014024del	NCBI36
NG_008969.1:g.11944del , LRG_460:g.11944del

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.446-61del
ENST00000528641.7:c.280-61del	ENSP00000434982.3:n.280-61del
ENST00000529797.2:n.920del
ENST00000682324.1:c.468+522del	ENSP00000508017.1:n.468+522del
ENST00000682659.1:c.100-61del	ENSP00000507351.1:n.100-61del
ENST00000682699.1:c.469-61del	ENSP00000507935.1:n.469-61del
ENST00000683237.1:c.469-61del	ENSP00000507343.1:n.469-61del
ENST00000683856.1:c.292-61del	ENSP00000507979.1:n.292-61del
ENST00000684006.1:c.469-61del	ENSP00000507269.1:n.469-61del
ENST00000684657.1:c.289-61del	ENSP00000507961.1:n.289-61del
ENST00000279146.8:c.469-61del MANE Select	ENSP00000279146.3:n.469-61del
ENST00000279146.7:c.469-61del	ENSP00000279146.3:n.469-61del
ENST00000525341.1:c.121-61del	ENSP00000476993.1:n.121-61del
ENST00000528641.6:c.280-61del	ENSP00000434982.2:n.280-61del
NM_001302959.1:c.292-61del	NP_001289888.1:n.292-61del
NM_001302960.1:c.469-61del	NP_001289889.1:n.469-61del
NM_003977.3:c.469-61del	NP_003968.3:n.469-61del
XM_024448761.1:c.469-61del	XP_024304529.1:n.469-61del
NM_003977.4:c.469-61del MANE Select	NP_003968.3:n.469-61del
NM_001302960.2:c.469-61del	NP_001289889.1:n.469-61del
NM_001302959.2:c.292-61del	NP_001289888.1:n.292-61del