Canonical Allele Identifier: CA1905833053
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130276C= , CM000672.2:g.43130276C= GRCh38
NC_000010.10:g.43625724C= , CM000672.1:g.43625724C= GRCh37
NC_000010.9:g.42945730C= NCBI36
NG_007489.1:g.58208C= , LRG_518:g.58208C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2007C= MANE Select ENSP00000347942.3:n.*2007C=
ENST00000355710.7:c.*2007C= ENSP00000347942.3:n.*2007C=
ENST00000615310.4:c.*2701C= ENSP00000480088.1:n.*2701C=
NM_020975.4:c.*2007C= , LRG_518t1:c.*2007C= NP_066124.1:n.*2007C=
XM_011540027.1:c.*775C= XP_011538329.1:n.*775C=
NM_020975.5:c.*2007C= NP_066124.1:n.*2007C=
NM_020975.6:c.*2007C= MANE Select NP_066124.1:n.*2007C=