Canonical Allele Identifier: CA2840623727

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489439_67489440insTCTC , CM000673.2:g.67489439_67489440insTCTC	GRCh38
NC_000011.9:g.67256910_67256911insTCTC , CM000673.1:g.67256910_67256911insTCTC	GRCh37
NC_000011.8:g.67013486_67013487insTCTC	NCBI36
NG_008969.1:g.11406_11407insTCTC , LRG_460:g.11406_11407insTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.429_430insTCTC
ENST00000528641.7:c.280-599_280-598insTCTC	ENSP00000434982.3:n.280-599_280-598insTCTC
ENST00000529797.2:n.382_383insTCTC
ENST00000682324.1:c.452_453insTCTC	ENSP00000508017.1:p.Met152LeufsTer?
ENST00000682659.1:c.100-599_100-598insTCTC	ENSP00000507351.1:n.100-599_100-598insTCTC
ENST00000682699.1:c.452_453insTCTC	ENSP00000507935.1:p.Met152LeufsTer?
ENST00000683237.1:c.452_453insTCTC	ENSP00000507343.1:p.Met152LeufsTer?
ENST00000683856.1:c.275_276insTCTC	ENSP00000507979.1:p.Met93LeufsTer?
ENST00000684006.1:c.452_453insTCTC	ENSP00000507269.1:p.Met152LeufsTer?
ENST00000684657.1:c.272_273insTCTC	ENSP00000507961.1:p.Met92LeufsTer?
ENST00000279146.8:c.452_453insTCTC MANE Select	ENSP00000279146.3:p.Met152LeufsTer?
ENST00000279146.7:c.452_453insTCTC	ENSP00000279146.3:p.Met152LeufsTer?
ENST00000525341.1:c.104_105insTCTC	ENSP00000476993.1:p.Met36LeufsTer?
ENST00000528641.6:c.280-599_280-598insTCTC	ENSP00000434982.2:n.280-599_280-598insTCTC
ENST00000529797.1:n.562_563insTCTC
NM_001302959.1:c.275_276insTCTC	NP_001289888.1:p.Met93LeufsTer?
NM_001302960.1:c.452_453insTCTC	NP_001289889.1:p.Met152LeufsTer?
NM_003977.3:c.452_453insTCTC	NP_003968.3:p.Met152LeufsTer?
XM_024448761.1:c.452_453insTCTC	XP_024304529.1:p.Met152LeufsTer?
NM_003977.4:c.452_453insTCTC MANE Select	NP_003968.3:p.Met152LeufsTer?
NM_001302960.2:c.452_453insTCTC	NP_001289889.1:p.Met152LeufsTer?
NM_001302959.2:c.275_276insTCTC	NP_001289888.1:p.Met93LeufsTer?