Canonical Allele Identifier: CA009273
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13925
ClinVar RCV Id: RCV000014950 RCV001206325
dbSNP Id: rs76449634
MyVariant Identifiers: chr10:g.43597990C>T (hg19) chr10:g.43102542C>T (hg38)
PubMed: PMID:8114939
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43102542C>T , CM000672.2:g.43102542C>T GRCh38
NC_000010.10:g.43597990C>T , CM000672.1:g.43597990C>T GRCh37
NC_000010.9:g.42917996C>T NCBI36
NG_007489.1:g.30474C>T , LRG_518:g.30474C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.538C>T ENSP00000480088.2:p.Arg180Ter
ENST00000683278.1:c.459C>T
ENST00000684216.1:c.440C>T
ENST00000340058.6:c.538C>T ENSP00000344798.4:p.Arg180Ter
ENST00000355710.8:c.538C>T MANE Select ENSP00000347942.3:p.Arg180Ter
ENST00000638465.1:c.480C>T
ENST00000640619.1:c.311C>T
ENST00000671844.1:c.538C>T ENSP00000500541.1:p.Arg180Ter
ENST00000672389.1:c.74-8665C>T ENSP00000500252.1:n.74-8665C>T
ENST00000340058.5:c.538C>T ENSP00000344798.4:p.Arg180Ter
ENST00000355710.7:c.538C>T ENSP00000347942.3:p.Arg180Ter
ENST00000498820.5:c.74-9557C>T ENSP00000419080.1:n.74-9557C>T
ENST00000615310.4:c.538C>T ENSP00000480088.1:p.Arg180Ter
NM_020630.4:c.538C>T , LRG_518t2:c.538C>T NP_065681.1:p.Arg180Ter
NM_020975.4:c.538C>T , LRG_518t1:c.538C>T NP_066124.1:p.Arg180Ter
XM_011540027.1:c.538C>T XP_011538329.1:p.Arg180Ter
NM_020630.5:c.538C>T NP_065681.1:p.Arg180Ter
NM_020975.5:c.538C>T NP_066124.1:p.Arg180Ter
NM_020975.6:c.538C>T MANE Select NP_066124.1:p.Arg180Ter
NM_020630.6:c.538C>T NP_065681.1:p.Arg180Ter
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