Canonical Allele Identifier: CA1905813065
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43113638G= , CM000672.2:g.43113638G= GRCh38
NC_000010.10:g.43609086G= , CM000672.1:g.43609086G= GRCh37
NC_000010.9:g.42929092G= NCBI36
NG_007489.1:g.41570G= , LRG_518:g.41570G=

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1446G= ENSP00000480088.2:p.Glu482=
ENST00000683007.1:n.1416G=
ENST00000683872.1:n.603G=
ENST00000340058.6:c.1842G= ENSP00000344798.4:p.Glu614=
ENST00000355710.8:c.1842G= MANE Select ENSP00000347942.3:p.Glu614=
ENST00000671844.1:c.*436G= ENSP00000500541.1:n.*436G=
ENST00000672389.1:c.*436G= ENSP00000500252.1:n.*436G=
ENST00000340058.5:c.1842G= ENSP00000344798.4:p.Glu614=
ENST00000355710.7:c.1842G= ENSP00000347942.3:p.Glu614=
ENST00000498820.5:c.393G= ENSP00000419080.1:p.Glu131=
ENST00000615310.4:c.1289+2406G= ENSP00000480088.1:n.1289+2406G=
NM_020630.4:c.1842G= , LRG_518t2:c.1842G= NP_065681.1:p.Glu614=
NM_020975.4:c.1842G= , LRG_518t1:c.1842G= NP_066124.1:p.Glu614=
XM_011540027.1:c.1842G= XP_011538329.1:p.Glu614=
NM_001355216.1:c.1080G= NP_001342145.1:p.Glu360=
NM_020630.5:c.1842G= NP_065681.1:p.Glu614=
NM_020975.5:c.1842G= NP_066124.1:p.Glu614=
NM_020975.6:c.1842G= MANE Select NP_066124.1:p.Glu614=
NM_020630.6:c.1842G= NP_065681.1:p.Glu614=