Canonical Allele Identifier: CA1905813475
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43114500T= , CM000672.2:g.43114500T= GRCh38
NC_000010.10:g.43609948T= , CM000672.1:g.43609948T= GRCh37
NC_000010.9:g.42929954T= NCBI36
NG_007489.1:g.42432T= , LRG_518:g.42432T=

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1504T= ENSP00000480088.2:p.Cys502=
ENST00000683007.1:n.1474T=
ENST00000683872.1:n.1465T=
ENST00000340058.6:c.1900T= ENSP00000344798.4:p.Cys634=
ENST00000355710.8:c.1900T= MANE Select ENSP00000347942.3:p.Cys634=
ENST00000671844.1:c.*494T= ENSP00000500541.1:n.*494T=
ENST00000672389.1:c.*494T= ENSP00000500252.1:n.*494T=
ENST00000340058.5:c.1900T= ENSP00000344798.4:p.Cys634=
ENST00000355710.7:c.1900T= ENSP00000347942.3:p.Cys634=
ENST00000498820.5:c.451T= ENSP00000419080.1:p.Cys151=
ENST00000615310.4:c.1289+3268T= ENSP00000480088.1:n.1289+3268T=
NM_020630.4:c.1900T= , LRG_518t2:c.1900T= NP_065681.1:p.Cys634=
NM_020975.4:c.1900T= , LRG_518t1:c.1900T= NP_066124.1:p.Cys634=
XM_011540027.1:c.1900T= XP_011538329.1:p.Cys634=
NM_001355216.1:c.1138T= NP_001342145.1:p.Cys380=
NM_020630.5:c.1900T= NP_065681.1:p.Cys634=
NM_020975.5:c.1900T= NP_066124.1:p.Cys634=
NM_020975.6:c.1900T= MANE Select NP_066124.1:p.Cys634=
NM_020630.6:c.1900T= NP_065681.1:p.Cys634=