Canonical Allele Identifier: CA2787743873
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43118301C>T , CM000672.2:g.43118301C>T GRCh38
NC_000010.10:g.43613749C>T , CM000672.1:g.43613749C>T GRCh37
NC_000010.9:g.42933755C>T NCBI36
NG_007489.1:g.46233C>T , LRG_518:g.46233C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1889-72C>T ENSP00000480088.2:n.1889-72C>T
ENST00000683007.1:n.1859-72C>T
ENST00000683872.1:n.1850-72C>T
ENST00000340058.6:c.2285-72C>T ENSP00000344798.4:n.2285-72C>T
ENST00000355710.8:c.2285-72C>T MANE Select ENSP00000347942.3:n.2285-72C>T
ENST00000671844.1:c.*879-72C>T ENSP00000500541.1:n.*879-72C>T
ENST00000672389.1:c.*879-72C>T ENSP00000500252.1:n.*879-72C>T
ENST00000340058.5:c.2285-72C>T ENSP00000344798.4:n.2285-72C>T
ENST00000355710.7:c.2285-72C>T ENSP00000347942.3:n.2285-72C>T
ENST00000615310.4:c.1290-1401C>T ENSP00000480088.1:n.1290-1401C>T
NM_020630.4:c.2285-72C>T , LRG_518t2:c.2285-72C>T NP_065681.1:n.2285-72C>T
NM_020975.4:c.2285-72C>T , LRG_518t1:c.2285-72C>T NP_066124.1:n.2285-72C>T
XM_011540027.1:c.2285-72C>T XP_011538329.1:n.2285-72C>T
NM_001355216.1:c.1523-72C>T NP_001342145.1:n.1523-72C>T
NM_020630.5:c.2285-72C>T NP_065681.1:n.2285-72C>T
NM_020975.5:c.2285-72C>T NP_066124.1:n.2285-72C>T
NM_020975.6:c.2285-72C>T MANE Select NP_066124.1:n.2285-72C>T
NM_020630.6:c.2285-72C>T NP_065681.1:n.2285-72C>T