Canonical Allele Identifier: CA2614625148

Gene: AIP

Linked Data

• gnomAD v4: 11-67490618-TGTGCCAATGAAGCATGAATGGTGTATTGGGGGTGGGGTGGCATCCTCAGGTCAGGGAGGGCTCTCTCTCCCCTGTGGGCCCATG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490625_67490708del , CM000673.2:g.67490625_67490708del	GRCh38
NC_000011.9:g.67258096_67258179del , CM000673.1:g.67258096_67258179del	GRCh37
NC_000011.8:g.67014672_67014755del	NCBI36
NG_008969.1:g.12592_12675del , LRG_460:g.12592_12675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.932_1015del
ENST00000528641.7:c.599-163_599-80del	ENSP00000434982.3:n.599-163_599-80del
ENST00000529797.2:n.1467_1550del
ENST00000682324.1:c.469-372_469-289del	ENSP00000508017.1:n.469-372_469-289del
ENST00000682659.1:c.419-163_419-80del	ENSP00000507351.1:n.419-163_419-80del
ENST00000682699.1:c.788-163_788-80del	ENSP00000507935.1:n.788-163_788-80del
ENST00000683237.1:c.780-163_780-80del	ENSP00000507343.1:n.780-163_780-80del
ENST00000683856.1:c.611-163_611-80del	ENSP00000507979.1:n.611-163_611-80del
ENST00000684006.1:c.787+168_788-91del	ENSP00000507269.1:n.787+168_788-91del
ENST00000684657.1:c.608-163_608-80del	ENSP00000507961.1:n.608-163_608-80del
ENST00000279146.8:c.788-163_788-80del MANE Select	ENSP00000279146.3:n.788-163_788-80del
ENST00000279146.7:c.788-163_788-80del	ENSP00000279146.3:n.788-163_788-80del
ENST00000528641.6:c.599-163_599-80del	ENSP00000434982.2:n.599-163_599-80del
NM_001302959.1:c.611-163_611-80del	NP_001289888.1:n.611-163_611-80del
NM_001302960.1:c.780-163_780-80del	NP_001289889.1:n.780-163_780-80del
NM_003977.3:c.788-163_788-80del	NP_003968.3:n.788-163_788-80del
XM_024448761.1:c.788-163_788-80del	XP_024304529.1:n.788-163_788-80del
NM_003977.4:c.788-163_788-80del MANE Select	NP_003968.3:n.788-163_788-80del
NM_001302960.2:c.780-163_780-80del	NP_001289889.1:n.780-163_780-80del
NM_001302959.2:c.611-163_611-80del	NP_001289888.1:n.611-163_611-80del