Canonical Allele Identifier: CA008334
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs377767409

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43114501_43114502delinsTG , CM000672.2:g.43114501_43114502delinsTG GRCh38
NC_000010.10:g.43609949_43609950delinsTG , CM000672.1:g.43609949_43609950delinsTG GRCh37
NC_000010.9:g.42929955_42929956delinsTG NCBI36
NG_007489.1:g.42433_42434delinsTG , LRG_518:g.42433_42434delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1505_1506delinsTG ENSP00000480088.2:p.Cys502Leu
ENST00000683007.1:n.1475_1476delinsTG
ENST00000683872.1:n.1466_1467delinsTG
ENST00000340058.6:c.1901_1902delinsTG ENSP00000344798.4:p.Cys634Leu
ENST00000355710.8:c.1901_1902delinsTG MANE Select ENSP00000347942.3:p.Cys634Leu
ENST00000671844.1:c.*495_*496delinsTG ENSP00000500541.1:n.*495_*496delinsTG
ENST00000672389.1:c.*495_*496delinsTG ENSP00000500252.1:n.*495_*496delinsTG
ENST00000340058.5:c.1901_1902delinsTG ENSP00000344798.4:p.Cys634Leu
ENST00000355710.7:c.1901_1902delinsTG ENSP00000347942.3:p.Cys634Leu
ENST00000498820.5:c.452_453delinsTG ENSP00000419080.1:p.Cys151Leu
ENST00000615310.4:c.1289+3269_1289+3270delinsTG ENSP00000480088.1:n.1289+3269_1289+3270de...
NM_020630.4:c.1901_1902delinsTG , LRG_518t2:c.1901_1902delinsTG NP_065681.1:p.Cys634Leu
NM_020975.4:c.1901_1902delinsTG , LRG_518t1:c.1901_1902delinsTG NP_066124.1:p.Cys634Leu
XM_011540027.1:c.1901_1902delinsTG XP_011538329.1:p.Cys634Leu
NM_001355216.1:c.1139_1140delinsTG NP_001342145.1:p.Cys380Leu
NM_020630.5:c.1901_1902delinsTG NP_065681.1:p.Cys634Leu
NM_020975.5:c.1901_1902delinsTG NP_066124.1:p.Cys634Leu
NM_020975.6:c.1901_1902delinsTG MANE Select NP_066124.1:p.Cys634Leu
NM_020630.6:c.1901_1902delinsTG NP_065681.1:p.Cys634Leu