Canonical Allele Identifier: CA2608869627
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43106288G>T , CM000672.2:g.43106288G>T GRCh38
NC_000010.10:g.43601736G>T , CM000672.1:g.43601736G>T GRCh37
NC_000010.9:g.42921742G>T NCBI36
NG_007489.1:g.34220G>T , LRG_518:g.34220G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.867+1095G>T ENSP00000480088.2:n.867+1095G>T
ENST00000683007.1:n.442-88G>T
ENST00000340058.6:c.868-88G>T ENSP00000344798.4:n.868-88G>T
ENST00000355710.8:c.868-88G>T MANE Select ENSP00000347942.3:n.868-88G>T
ENST00000671844.1:c.625+3659G>T ENSP00000500541.1:n.625+3659G>T
ENST00000672389.1:c.74-4919G>T ENSP00000500252.1:n.74-4919G>T
ENST00000340058.5:c.868-88G>T ENSP00000344798.4:n.868-88G>T
ENST00000355710.7:c.868-88G>T ENSP00000347942.3:n.868-88G>T
ENST00000479913.1:n.463-88G>T
ENST00000498820.5:c.74-5811G>T ENSP00000419080.1:n.74-5811G>T
ENST00000615310.4:c.868-88G>T ENSP00000480088.1:n.868-88G>T
NM_020630.4:c.868-88G>T , LRG_518t2:c.868-88G>T NP_065681.1:n.868-88G>T
NM_020975.4:c.868-88G>T , LRG_518t1:c.868-88G>T NP_066124.1:n.868-88G>T
XM_011540027.1:c.868-88G>T XP_011538329.1:n.868-88G>T
NM_001355216.1:c.106-88G>T NP_001342145.1:n.106-88G>T
NM_020630.5:c.868-88G>T NP_065681.1:n.868-88G>T
NM_020975.5:c.868-88G>T NP_066124.1:n.868-88G>T
NM_020975.6:c.868-88G>T MANE Select NP_066124.1:n.868-88G>T
NM_020630.6:c.868-88G>T NP_065681.1:n.868-88G>T