Canonical Allele Identifier: CA1905833039
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130265A= , CM000672.2:g.43130265A= GRCh38
NC_000010.10:g.43625713A= , CM000672.1:g.43625713A= GRCh37
NC_000010.9:g.42945719A= NCBI36
NG_007489.1:g.58197A= , LRG_518:g.58197A=

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3511A= ENSP00000480088.2:n.*3511A=
ENST00000683007.1:n.6304A=
ENST00000355710.8:c.*1996A= MANE Select ENSP00000347942.3:n.*1996A=
ENST00000355710.7:c.*1996A= ENSP00000347942.3:n.*1996A=
ENST00000615310.4:c.*2690A= ENSP00000480088.1:n.*2690A=
NM_020975.4:c.*1996A= , LRG_518t1:c.*1996A= NP_066124.1:n.*1996A=
XM_011540027.1:c.*764A= XP_011538329.1:n.*764A=
NM_020975.5:c.*1996A= NP_066124.1:n.*1996A=
NM_020975.6:c.*1996A= MANE Select NP_066124.1:n.*1996A=