Canonical Allele Identifier: CA927682493
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1838417992

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130270A>T , CM000672.2:g.43130270A>T GRCh38
NC_000010.10:g.43625718A>T , CM000672.1:g.43625718A>T GRCh37
NC_000010.9:g.42945724A>T NCBI36
NG_007489.1:g.58202A>T , LRG_518:g.58202A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3516A>T ENSP00000480088.2:n.*3516A>T
ENST00000683007.1:n.6309A>T
ENST00000355710.8:c.*2001A>T MANE Select ENSP00000347942.3:n.*2001A>T
ENST00000355710.7:c.*2001A>T ENSP00000347942.3:n.*2001A>T
ENST00000615310.4:c.*2695A>T ENSP00000480088.1:n.*2695A>T
NM_020975.4:c.*2001A>T , LRG_518t1:c.*2001A>T NP_066124.1:n.*2001A>T
XM_011540027.1:c.*769A>T XP_011538329.1:n.*769A>T
NM_020975.5:c.*2001A>T NP_066124.1:n.*2001A>T
NM_020975.6:c.*2001A>T MANE Select NP_066124.1:n.*2001A>T