Canonical Allele Identifier: CA1980172375

Gene: AIP MIR6752

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490264C= , CM000673.2:g.67490264C=	GRCh38
NC_000011.9:g.67257735C= , CM000673.1:g.67257735C=	GRCh37
NC_000011.8:g.67014311C=	NCBI36
NG_008969.1:g.12231C= , LRG_460:g.12231C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.622+50C= (AIP)
ENST00000528641.7:c.456+50C= (AIP)	ENSP00000434982.3:n.456+50C=
ENST00000529797.2:n.1157+50C= (AIP)
ENST00000682324.1:c.469-733C= (AIP)	ENSP00000508017.1:n.469-733C=
ENST00000682659.1:c.276+50C= (AIP)	ENSP00000507351.1:n.276+50C=
ENST00000682699.1:c.645+50C= (AIP)	ENSP00000507935.1:n.645+50C=
ENST00000683237.1:c.645+50C= (AIP)	ENSP00000507343.1:n.645+50C=
ENST00000683856.1:c.468+50C= (AIP)	ENSP00000507979.1:n.468+50C=
ENST00000684006.1:c.645+50C= (AIP)	ENSP00000507269.1:n.645+50C=
ENST00000684657.1:c.465+50C= (AIP)	ENSP00000507961.1:n.465+50C=
ENST00000279146.8:c.645+50C= (AIP) MANE Select	ENSP00000279146.3:n.645+50C=
ENST00000279146.7:c.645+50C= (AIP)	ENSP00000279146.3:n.645+50C=
ENST00000525341.1:c.297+50C= (AIP)	ENSP00000476993.1:n.297+50C=
ENST00000528641.6:c.456+50C= (AIP)	ENSP00000434982.2:n.456+50C=
NM_001302959.1:c.468+50C= (AIP)	NP_001289888.1:n.468+50C=
NM_001302960.1:c.645+50C= (AIP)	NP_001289889.1:n.645+50C=
NM_003977.3:c.645+50C= (AIP)	NP_003968.3:n.645+50C=
NR_106810.1:n.20C= (MIR6752)
XM_024448761.1:c.645+50C= (AIP)	XP_024304529.1:n.645+50C=
NM_003977.4:c.645+50C= (AIP) MANE Select	NP_003968.3:n.645+50C=
NM_001302960.2:c.645+50C= (AIP)	NP_001289889.1:n.645+50C=
NM_001302959.2:c.468+50C= (AIP)	NP_001289888.1:n.468+50C=