Canonical Allele Identifier: CA2721588217
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1466377483

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43113546C>T , CM000672.2:g.43113546C>T GRCh38
NC_000010.10:g.43608994C>T , CM000672.1:g.43608994C>T GRCh37
NC_000010.9:g.42929000C>T NCBI36
NG_007489.1:g.41478C>T , LRG_518:g.41478C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1364-10C>T ENSP00000480088.2:n.1364-10C>T
ENST00000683007.1:n.1334-10C>T
ENST00000683872.1:n.521-10C>T
ENST00000340058.6:c.1760-10C>T ENSP00000344798.4:n.1760-10C>T
ENST00000355710.8:c.1760-10C>T MANE Select ENSP00000347942.3:n.1760-10C>T
ENST00000671844.1:c.*354-10C>T ENSP00000500541.1:n.*354-10C>T
ENST00000672389.1:c.*354-10C>T ENSP00000500252.1:n.*354-10C>T
ENST00000340058.5:c.1760-10C>T ENSP00000344798.4:n.1760-10C>T
ENST00000355710.7:c.1760-10C>T ENSP00000347942.3:n.1760-10C>T
ENST00000498820.5:c.311-10C>T ENSP00000419080.1:n.311-10C>T
ENST00000615310.4:c.1289+2314C>T ENSP00000480088.1:n.1289+2314C>T
NM_020630.4:c.1760-10C>T , LRG_518t2:c.1760-10C>T NP_065681.1:n.1760-10C>T
NM_020975.4:c.1760-10C>T , LRG_518t1:c.1760-10C>T NP_066124.1:n.1760-10C>T
XM_011540027.1:c.1760-10C>T XP_011538329.1:n.1760-10C>T
NM_001355216.1:c.998-10C>T NP_001342145.1:n.998-10C>T
NM_020630.5:c.1760-10C>T NP_065681.1:n.1760-10C>T
NM_020975.5:c.1760-10C>T NP_066124.1:n.1760-10C>T
NM_020975.6:c.1760-10C>T MANE Select NP_066124.1:n.1760-10C>T
NM_020630.6:c.1760-10C>T NP_065681.1:n.1760-10C>T