Canonical Allele Identifier: CA376553074

Gene: RET

Linked Data

• ClinVar Variation Id: 1783841
• ClinVar RCV Id: RCV002423713
• dbSNP Id: rs1838023845
• MyVariant Identifiers: chr10:g.43610031C>G (hg19) ; chr10:g.43114583C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114583C>G , CM000672.2:g.43114583C>G	GRCh38
NC_000010.10:g.43610031C>G , CM000672.1:g.43610031C>G	GRCh37
NC_000010.9:g.42930037C>G	NCBI36
NG_007489.1:g.42515C>G , LRG_518:g.42515C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1587C>G	ENSP00000480088.2:p.His529Gln
ENST00000683007.1:n.1557C>G
ENST00000683872.1:n.1548C>G
ENST00000340058.6:c.1983C>G	ENSP00000344798.4:p.His661Gln
ENST00000355710.8:c.1983C>G MANE Select	ENSP00000347942.3:p.His661Gln
ENST00000671844.1:c.*577C>G	ENSP00000500541.1:n.*577C>G
ENST00000672389.1:c.*577C>G	ENSP00000500252.1:n.*577C>G
ENST00000340058.5:c.1983C>G	ENSP00000344798.4:p.His661Gln
ENST00000355710.7:c.1983C>G	ENSP00000347942.3:p.His661Gln
ENST00000498820.5:c.534C>G	ENSP00000419080.1:p.His178Gln
ENST00000615310.4:c.1289+3351C>G	ENSP00000480088.1:n.1289+3351C>G
NM_020630.4:c.1983C>G , LRG_518t2:c.1983C>G	NP_065681.1:p.His661Gln
NM_020975.4:c.1983C>G , LRG_518t1:c.1983C>G	NP_066124.1:p.His661Gln
XM_011540027.1:c.1983C>G	XP_011538329.1:p.His661Gln
NM_001355216.1:c.1221C>G	NP_001342145.1:p.His407Gln
NM_020630.5:c.1983C>G	NP_065681.1:p.His661Gln
NM_020975.5:c.1983C>G	NP_066124.1:p.His661Gln
NM_020975.6:c.1983C>G MANE Select	NP_066124.1:p.His661Gln
NM_020630.6:c.1983C>G	NP_065681.1:p.His661Gln