Canonical Allele Identifier: CA1905833056
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130280A= , CM000672.2:g.43130280A= GRCh38
NC_000010.10:g.43625728A= , CM000672.1:g.43625728A= GRCh37
NC_000010.9:g.42945734A= NCBI36
NG_007489.1:g.58212A= , LRG_518:g.58212A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2011A= MANE Select ENSP00000347942.3:n.*2011A=
ENST00000355710.7:c.*2011A= ENSP00000347942.3:n.*2011A=
ENST00000615310.4:c.*2705A= ENSP00000480088.1:n.*2705A=
NM_020975.4:c.*2011A= , LRG_518t1:c.*2011A= NP_066124.1:n.*2011A=
XM_011540027.1:c.*779A= XP_011538329.1:n.*779A=
NM_020975.5:c.*2011A= NP_066124.1:n.*2011A=
NM_020975.6:c.*2011A= MANE Select NP_066124.1:n.*2011A=