Canonical Allele Identifier: CA1905833019
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130230G= , CM000672.2:g.43130230G= GRCh38
NC_000010.10:g.43625678G= , CM000672.1:g.43625678G= GRCh37
NC_000010.9:g.42945684G= NCBI36
NG_007489.1:g.58162G= , LRG_518:g.58162G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.*3476G= ENSP00000480088.2:n.*3476G=
ENST00000683007.1:n.6269G=
ENST00000355710.8:c.*1961G= MANE Select ENSP00000347942.3:n.*1961G=
ENST00000355710.7:c.*1961G= ENSP00000347942.3:n.*1961G=
ENST00000615310.4:c.*2655G= ENSP00000480088.1:n.*2655G=
NM_020975.4:c.*1961G= , LRG_518t1:c.*1961G= NP_066124.1:n.*1961G=
XM_011540027.1:c.*729G= XP_011538329.1:n.*729G=
NM_020975.5:c.*1961G= NP_066124.1:n.*1961G=
NM_020975.6:c.*1961G= MANE Select NP_066124.1:n.*1961G=