Canonical Allele Identifier: CA2741182862

Gene: AIP MIR6752

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490245_67490246insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC , CM000673.2:g.67490245_67490246insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC	GRCh38
NC_000011.9:g.67257716_67257717insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC , CM000673.1:g.67257716_67257717insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC	GRCh37
NC_000011.8:g.67014292_67014293insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC	NCBI36
NG_008969.1:g.12212_12213insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC , LRG_460:g.12212_12213insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.622+31_622+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)
ENST00000528641.7:c.456+31_456+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000434982.3:n.456+31_456+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000529797.2:n.1157+31_1157+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)
ENST00000682324.1:c.469-752_469-751insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000508017.1:n.469-752_469-751insCATCCCAGCCAGAGGAACCTCAA...
ENST00000682659.1:c.276+31_276+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000507351.1:n.276+31_276+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000682699.1:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000507935.1:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000683237.1:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000507343.1:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000683856.1:c.468+31_468+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000507979.1:n.468+31_468+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000684006.1:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000507269.1:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000684657.1:c.465+31_465+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000507961.1:n.465+31_465+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000279146.8:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP) MANE Select	ENSP00000279146.3:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000279146.7:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000279146.3:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000525341.1:c.297+31_297+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000476993.1:n.297+31_297+32insCATCCCAGCCAGAGGAACCTCAAAT...
ENST00000528641.6:c.456+31_456+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	ENSP00000434982.2:n.456+31_456+32insCATCCCAGCCAGAGGAACCTCAAAT...
NM_001302959.1:c.468+31_468+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	NP_001289888.1:n.468+31_468+32insCATCCCAGCCAGAGGAACCTCAAATGCT...
NM_001302960.1:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	NP_001289889.1:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCT...
NM_003977.3:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	NP_003968.3:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAA...
NR_106810.1:n.1_2insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (MIR6752)
XM_024448761.1:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	XP_024304529.1:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCT...
NM_003977.4:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP) MANE Select	NP_003968.3:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAA...
NM_001302960.2:c.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	NP_001289889.1:n.645+31_645+32insCATCCCAGCCAGAGGAACCTCAAATGCT...
NM_001302959.2:c.468+31_468+32insCATCCCAGCCAGAGGAACCTCAAATGCTAAAGAGCGAGAGGGAGGCTGC (AIP)	NP_001289888.1:n.468+31_468+32insCATCCCAGCCAGAGGAACCTCAAATGCT...