Canonical Allele Identifier: CA376552771

Gene: RET

Linked Data

• ClinVar Variation Id: 2166006
• ClinVar RCV Id: RCV003090274 ; RCV003294495
• gnomAD v4: 10-43113630-T-C
• MyVariant Identifiers: chr10:g.43609078T>C (hg19) ; chr10:g.43113630T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113630T>C , CM000672.2:g.43113630T>C	GRCh38
NC_000010.10:g.43609078T>C , CM000672.1:g.43609078T>C	GRCh37
NC_000010.9:g.42929084T>C	NCBI36
NG_007489.1:g.41562T>C , LRG_518:g.41562T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1438T>C	ENSP00000480088.2:p.Phe480Leu
ENST00000683007.1:n.1408T>C
ENST00000683872.1:n.595T>C
ENST00000340058.6:c.1834T>C	ENSP00000344798.4:p.Phe612Leu
ENST00000355710.8:c.1834T>C MANE Select	ENSP00000347942.3:p.Phe612Leu
ENST00000671844.1:c.*428T>C	ENSP00000500541.1:n.*428T>C
ENST00000672389.1:c.*428T>C	ENSP00000500252.1:n.*428T>C
ENST00000340058.5:c.1834T>C	ENSP00000344798.4:p.Phe612Leu
ENST00000355710.7:c.1834T>C	ENSP00000347942.3:p.Phe612Leu
ENST00000498820.5:c.385T>C	ENSP00000419080.1:p.Phe129Leu
ENST00000615310.4:c.1289+2398T>C	ENSP00000480088.1:n.1289+2398T>C
NM_020630.4:c.1834T>C , LRG_518t2:c.1834T>C	NP_065681.1:p.Phe612Leu
NM_020975.4:c.1834T>C , LRG_518t1:c.1834T>C	NP_066124.1:p.Phe612Leu
XM_011540027.1:c.1834T>C	XP_011538329.1:p.Phe612Leu
NM_001355216.1:c.1072T>C	NP_001342145.1:p.Phe358Leu
NM_020630.5:c.1834T>C	NP_065681.1:p.Phe612Leu
NM_020975.5:c.1834T>C	NP_066124.1:p.Phe612Leu
NM_020975.6:c.1834T>C MANE Select	NP_066124.1:p.Phe612Leu
NM_020630.6:c.1834T>C	NP_065681.1:p.Phe612Leu