Canonical Allele Identifier: CA2608869767
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43124822G>T , CM000672.2:g.43124822G>T GRCh38
NC_000010.10:g.43620270G>T , CM000672.1:g.43620270G>T GRCh37
NC_000010.9:g.42940276G>T NCBI36
NG_007489.1:g.52754G>T , LRG_518:g.52754G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.2544-61G>T ENSP00000480088.2:n.2544-61G>T
ENST00000683007.1:n.2514-61G>T
ENST00000340058.6:c.2940-61G>T ENSP00000344798.4:n.2940-61G>T
ENST00000355710.8:c.2940-61G>T MANE Select ENSP00000347942.3:n.2940-61G>T
ENST00000671844.1:c.*1534-61G>T ENSP00000500541.1:n.*1534-61G>T
ENST00000672389.1:c.*1534-61G>T ENSP00000500252.1:n.*1534-61G>T
ENST00000340058.5:c.2940-61G>T ENSP00000344798.4:n.2940-61G>T
ENST00000355710.7:c.2940-61G>T ENSP00000347942.3:n.2940-61G>T
ENST00000615310.4:c.*289-61G>T ENSP00000480088.1:n.*289-61G>T
NM_020630.4:c.2940-61G>T , LRG_518t2:c.2940-61G>T NP_065681.1:n.2940-61G>T
NM_020975.4:c.2940-61G>T , LRG_518t1:c.2940-61G>T NP_066124.1:n.2940-61G>T
XM_011540027.1:c.2940-61G>T XP_011538329.1:n.2940-61G>T
NM_001355216.1:c.2178-61G>T NP_001342145.1:n.2178-61G>T
NM_020630.5:c.2940-61G>T NP_065681.1:n.2940-61G>T
NM_020975.5:c.2940-61G>T NP_066124.1:n.2940-61G>T
NM_020975.6:c.2940-61G>T MANE Select NP_066124.1:n.2940-61G>T
NM_020630.6:c.2940-61G>T NP_065681.1:n.2940-61G>T