Canonical Allele Identifier: CA1980172366

Gene: AIP MIR6752

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490251G= , CM000673.2:g.67490251G=	GRCh38
NC_000011.9:g.67257722G= , CM000673.1:g.67257722G=	GRCh37
NC_000011.8:g.67014298G=	NCBI36
NG_008969.1:g.12218G= , LRG_460:g.12218G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.622+37G= (AIP)
ENST00000528641.7:c.456+37G= (AIP)	ENSP00000434982.3:n.456+37G=
ENST00000529797.2:n.1157+37G= (AIP)
ENST00000682324.1:c.469-746G= (AIP)	ENSP00000508017.1:n.469-746G=
ENST00000682659.1:c.276+37G= (AIP)	ENSP00000507351.1:n.276+37G=
ENST00000682699.1:c.645+37G= (AIP)	ENSP00000507935.1:n.645+37G=
ENST00000683237.1:c.645+37G= (AIP)	ENSP00000507343.1:n.645+37G=
ENST00000683856.1:c.468+37G= (AIP)	ENSP00000507979.1:n.468+37G=
ENST00000684006.1:c.645+37G= (AIP)	ENSP00000507269.1:n.645+37G=
ENST00000684657.1:c.465+37G= (AIP)	ENSP00000507961.1:n.465+37G=
ENST00000279146.8:c.645+37G= (AIP) MANE Select	ENSP00000279146.3:n.645+37G=
ENST00000279146.7:c.645+37G= (AIP)	ENSP00000279146.3:n.645+37G=
ENST00000525341.1:c.297+37G= (AIP)	ENSP00000476993.1:n.297+37G=
ENST00000528641.6:c.456+37G= (AIP)	ENSP00000434982.2:n.456+37G=
NM_001302959.1:c.468+37G= (AIP)	NP_001289888.1:n.468+37G=
NM_001302960.1:c.645+37G= (AIP)	NP_001289889.1:n.645+37G=
NM_003977.3:c.645+37G= (AIP)	NP_003968.3:n.645+37G=
NR_106810.1:n.7G= (MIR6752)
XM_024448761.1:c.645+37G= (AIP)	XP_024304529.1:n.645+37G=
NM_003977.4:c.645+37G= (AIP) MANE Select	NP_003968.3:n.645+37G=
NM_001302960.2:c.645+37G= (AIP)	NP_001289889.1:n.645+37G=
NM_001302959.2:c.468+37G= (AIP)	NP_001289888.1:n.468+37G=