Canonical Allele Identifier: CA1905819979

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120179G= , CM000672.2:g.43120179G=	GRCh38
NC_000010.10:g.43615627G= , CM000672.1:g.43615627G=	GRCh37
NC_000010.9:g.42935633G=	NCBI36
NG_007489.1:g.48111G= , LRG_518:g.48111G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2310G=	ENSP00000480088.2:p.Glu770=
ENST00000683007.1:n.2280G=
ENST00000683872.1:n.2271G=
ENST00000340058.6:c.2706G=	ENSP00000344798.4:p.Glu902=
ENST00000355710.8:c.2706G= MANE Select	ENSP00000347942.3:p.Glu902=
ENST00000671844.1:c.*1300G=	ENSP00000500541.1:n.*1300G=
ENST00000672389.1:c.*1300G=	ENSP00000500252.1:n.*1300G=
ENST00000340058.5:c.2706G=	ENSP00000344798.4:p.Glu902=
ENST00000355710.7:c.2706G=	ENSP00000347942.3:p.Glu902=
ENST00000615310.4:c.*55G=	ENSP00000480088.1:n.*55G=
NM_020630.4:c.2706G= , LRG_518t2:c.2706G=	NP_065681.1:p.Glu902=
NM_020975.4:c.2706G= , LRG_518t1:c.2706G=	NP_066124.1:p.Glu902=
XM_011540027.1:c.2706G=	XP_011538329.1:p.Glu902=
NM_001355216.1:c.1944G=	NP_001342145.1:p.Glu648=
NM_020630.5:c.2706G=	NP_065681.1:p.Glu902=
NM_020975.5:c.2706G=	NP_066124.1:p.Glu902=
NM_020975.6:c.2706G= MANE Select	NP_066124.1:p.Glu902=
NM_020630.6:c.2706G=	NP_065681.1:p.Glu902=