Canonical Allele Identifier: CA665319359
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1207050073

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43118235A>C , CM000672.2:g.43118235A>C GRCh38
NC_000010.10:g.43613683A>C , CM000672.1:g.43613683A>C GRCh37
NC_000010.9:g.42933689A>C NCBI36
NG_007489.1:g.46167A>C , LRG_518:g.46167A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1889-138A>C ENSP00000480088.2:n.1889-138A>C
ENST00000683007.1:n.1859-138A>C
ENST00000683872.1:n.1850-138A>C
ENST00000340058.6:c.2285-138A>C ENSP00000344798.4:n.2285-138A>C
ENST00000355710.8:c.2285-138A>C MANE Select ENSP00000347942.3:n.2285-138A>C
ENST00000671844.1:c.*879-138A>C ENSP00000500541.1:n.*879-138A>C
ENST00000672389.1:c.*879-138A>C ENSP00000500252.1:n.*879-138A>C
ENST00000340058.5:c.2285-138A>C ENSP00000344798.4:n.2285-138A>C
ENST00000355710.7:c.2285-138A>C ENSP00000347942.3:n.2285-138A>C
ENST00000615310.4:c.1290-1467A>C ENSP00000480088.1:n.1290-1467A>C
NM_020630.4:c.2285-138A>C , LRG_518t2:c.2285-138A>C NP_065681.1:n.2285-138A>C
NM_020975.4:c.2285-138A>C , LRG_518t1:c.2285-138A>C NP_066124.1:n.2285-138A>C
XM_011540027.1:c.2285-138A>C XP_011538329.1:n.2285-138A>C
NM_001355216.1:c.1523-138A>C NP_001342145.1:n.1523-138A>C
NM_020630.5:c.2285-138A>C NP_065681.1:n.2285-138A>C
NM_020975.5:c.2285-138A>C NP_066124.1:n.2285-138A>C
NM_020975.6:c.2285-138A>C MANE Select NP_066124.1:n.2285-138A>C
NM_020630.6:c.2285-138A>C NP_065681.1:n.2285-138A>C