Canonical Allele Identifier: CA030900
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43106558C>T , CM000672.2:g.43106558C>T GRCh38
NC_000010.10:g.43602006C>T , CM000672.1:g.43602006C>T GRCh37
NC_000010.9:g.42922012C>T NCBI36
NG_007489.1:g.34490C>T , LRG_518:g.34490C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.867+1365C>T ENSP00000480088.2:n.867+1365C>T
ENST00000683007.1:n.624C>T
ENST00000340058.6:c.1050C>T ENSP00000344798.4:p.Thr350=
ENST00000355710.8:c.1050C>T MANE Select ENSP00000347942.3:p.Thr350=
ENST00000671844.1:c.625+3929C>T ENSP00000500541.1:n.625+3929C>T
ENST00000672389.1:c.74-4649C>T ENSP00000500252.1:n.74-4649C>T
ENST00000340058.5:c.1050C>T ENSP00000344798.4:p.Thr350=
ENST00000355710.7:c.1050C>T ENSP00000347942.3:p.Thr350=
ENST00000498820.5:c.74-5541C>T ENSP00000419080.1:n.74-5541C>T
ENST00000615310.4:c.1050C>T ENSP00000480088.1:p.Thr350=
NM_020630.4:c.1050C>T , LRG_518t2:c.1050C>T NP_065681.1:p.Thr350=
NM_020975.4:c.1050C>T , LRG_518t1:c.1050C>T NP_066124.1:p.Thr350=
XM_011540027.1:c.1050C>T XP_011538329.1:p.Thr350=
NM_001355216.1:c.288C>T NP_001342145.1:p.Thr96=
NM_020630.5:c.1050C>T NP_065681.1:p.Thr350=
NM_020975.5:c.1050C>T NP_066124.1:p.Thr350=
NM_020975.6:c.1050C>T MANE Select NP_066124.1:p.Thr350=
NM_020630.6:c.1050C>T NP_065681.1:p.Thr350=