Canonical Allele Identifier: CA376555898

Gene: RET

Linked Data

• ClinVar Variation Id: 477346
• ClinVar RCV Id: RCV000554041 ; RCV002456264
• dbSNP Id: rs1554819410
• MyVariant Identifiers: chr10:g.43613914C>T (hg19) ; chr10:g.43118466C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118466C>T , CM000672.2:g.43118466C>T	GRCh38
NC_000010.10:g.43613914C>T , CM000672.1:g.43613914C>T	GRCh37
NC_000010.9:g.42933920C>T	NCBI36
NG_007489.1:g.46398C>T , LRG_518:g.46398C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1982C>T	ENSP00000480088.2:p.Ala661Val
ENST00000683007.1:n.1952C>T
ENST00000683872.1:n.1943C>T
ENST00000340058.6:c.2378C>T	ENSP00000344798.4:p.Ala793Val
ENST00000355710.8:c.2378C>T MANE Select	ENSP00000347942.3:p.Ala793Val
ENST00000671844.1:c.*972C>T	ENSP00000500541.1:n.*972C>T
ENST00000672389.1:c.*972C>T	ENSP00000500252.1:n.*972C>T
ENST00000340058.5:c.2378C>T	ENSP00000344798.4:p.Ala793Val
ENST00000355710.7:c.2378C>T	ENSP00000347942.3:p.Ala793Val
ENST00000615310.4:c.1290-1236C>T	ENSP00000480088.1:n.1290-1236C>T
NM_020630.4:c.2378C>T , LRG_518t2:c.2378C>T	NP_065681.1:p.Ala793Val
NM_020975.4:c.2378C>T , LRG_518t1:c.2378C>T	NP_066124.1:p.Ala793Val
XM_011540027.1:c.2378C>T	XP_011538329.1:p.Ala793Val
NM_001355216.1:c.1616C>T	NP_001342145.1:p.Ala539Val
NM_020630.5:c.2378C>T	NP_065681.1:p.Ala793Val
NM_020975.5:c.2378C>T	NP_066124.1:p.Ala793Val
NM_020975.6:c.2378C>T MANE Select	NP_066124.1:p.Ala793Val
NM_020630.6:c.2378C>T	NP_065681.1:p.Ala793Val