Canonical Allele Identifier: CA1905813490
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43114515G= , CM000672.2:g.43114515G= GRCh38
NC_000010.10:g.43609963G= , CM000672.1:g.43609963G= GRCh37
NC_000010.9:g.42929969G= NCBI36
NG_007489.1:g.42447G= , LRG_518:g.42447G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1519G= ENSP00000480088.2:p.Ala507=
ENST00000683007.1:n.1489G=
ENST00000683872.1:n.1480G=
ENST00000340058.6:c.1915G= ENSP00000344798.4:p.Ala639=
ENST00000355710.8:c.1915G= MANE Select ENSP00000347942.3:p.Ala639=
ENST00000671844.1:c.*509G= ENSP00000500541.1:n.*509G=
ENST00000672389.1:c.*509G= ENSP00000500252.1:n.*509G=
ENST00000340058.5:c.1915G= ENSP00000344798.4:p.Ala639=
ENST00000355710.7:c.1915G= ENSP00000347942.3:p.Ala639=
ENST00000498820.5:c.466G= ENSP00000419080.1:p.Ala156=
ENST00000615310.4:c.1289+3283G= ENSP00000480088.1:n.1289+3283G=
NM_020630.4:c.1915G= , LRG_518t2:c.1915G= NP_065681.1:p.Ala639=
NM_020975.4:c.1915G= , LRG_518t1:c.1915G= NP_066124.1:p.Ala639=
XM_011540027.1:c.1915G= XP_011538329.1:p.Ala639=
NM_001355216.1:c.1153G= NP_001342145.1:p.Ala385=
NM_020630.5:c.1915G= NP_065681.1:p.Ala639=
NM_020975.5:c.1915G= NP_066124.1:p.Ala639=
NM_020975.6:c.1915G= MANE Select NP_066124.1:p.Ala639=
NM_020630.6:c.1915G= NP_065681.1:p.Ala639=