Canonical Allele Identifier: CA469027870

Gene: RET

Linked Data

• ClinVar Variation Id: 2683100
• ClinVar RCV Id: RCV003481967
• dbSNP Id: rs377767396
• MyVariant Identifiers: chr10:g.43609071C>T (hg19) ; chr10:g.43113623C>T (hg38)
• PubMed: PMID:28647780

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113623C>T , CM000672.2:g.43113623C>T	GRCh38
NC_000010.10:g.43609071C>T , CM000672.1:g.43609071C>T	GRCh37
NC_000010.9:g.42929077C>T	NCBI36
NG_007489.1:g.41555C>T , LRG_518:g.41555C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1431C>T	ENSP00000480088.2:p.Cys477=
ENST00000683007.1:n.1401C>T
ENST00000683872.1:n.588C>T
ENST00000340058.6:c.1827C>T	ENSP00000344798.4:p.Cys609=
ENST00000355710.8:c.1827C>T MANE Select	ENSP00000347942.3:p.Cys609=
ENST00000671844.1:c.*421C>T	ENSP00000500541.1:n.*421C>T
ENST00000672389.1:c.*421C>T	ENSP00000500252.1:n.*421C>T
ENST00000340058.5:c.1827C>T	ENSP00000344798.4:p.Cys609=
ENST00000355710.7:c.1827C>T	ENSP00000347942.3:p.Cys609=
ENST00000498820.5:c.378C>T	ENSP00000419080.1:p.Cys126=
ENST00000615310.4:c.1289+2391C>T	ENSP00000480088.1:n.1289+2391C>T
NM_020630.4:c.1827C>T , LRG_518t2:c.1827C>T	NP_065681.1:p.Cys609=
NM_020975.4:c.1827C>T , LRG_518t1:c.1827C>T	NP_066124.1:p.Cys609=
XM_011540027.1:c.1827C>T	XP_011538329.1:p.Cys609=
NM_001355216.1:c.1065C>T	NP_001342145.1:p.Cys355=
NM_020630.5:c.1827C>T	NP_065681.1:p.Cys609=
NM_020975.5:c.1827C>T	NP_066124.1:p.Cys609=
NM_020975.6:c.1827C>T MANE Select	NP_066124.1:p.Cys609=
NM_020630.6:c.1827C>T	NP_065681.1:p.Cys609=