Canonical Allele Identifier: CA376553071

Gene: RET

Linked Data

• ClinVar Variation Id: 1353140
• ClinVar RCV Id: RCV001869938
• dbSNP Id: rs1838023752
• gnomAD v4: 10-43114582-A-G
• MyVariant Identifiers: chr10:g.43610030A>G (hg19) ; chr10:g.43114582A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114582A>G , CM000672.2:g.43114582A>G	GRCh38
NC_000010.10:g.43610030A>G , CM000672.1:g.43610030A>G	GRCh37
NC_000010.9:g.42930036A>G	NCBI36
NG_007489.1:g.42514A>G , LRG_518:g.42514A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1586A>G	ENSP00000480088.2:p.His529Arg
ENST00000683007.1:n.1556A>G
ENST00000683872.1:n.1547A>G
ENST00000340058.6:c.1982A>G	ENSP00000344798.4:p.His661Arg
ENST00000355710.8:c.1982A>G MANE Select	ENSP00000347942.3:p.His661Arg
ENST00000671844.1:c.*576A>G	ENSP00000500541.1:n.*576A>G
ENST00000672389.1:c.*576A>G	ENSP00000500252.1:n.*576A>G
ENST00000340058.5:c.1982A>G	ENSP00000344798.4:p.His661Arg
ENST00000355710.7:c.1982A>G	ENSP00000347942.3:p.His661Arg
ENST00000498820.5:c.533A>G	ENSP00000419080.1:p.His178Arg
ENST00000615310.4:c.1289+3350A>G	ENSP00000480088.1:n.1289+3350A>G
NM_020630.4:c.1982A>G , LRG_518t2:c.1982A>G	NP_065681.1:p.His661Arg
NM_020975.4:c.1982A>G , LRG_518t1:c.1982A>G	NP_066124.1:p.His661Arg
XM_011540027.1:c.1982A>G	XP_011538329.1:p.His661Arg
NM_001355216.1:c.1220A>G	NP_001342145.1:p.His407Arg
NM_020630.5:c.1982A>G	NP_065681.1:p.His661Arg
NM_020975.5:c.1982A>G	NP_066124.1:p.His661Arg
NM_020975.6:c.1982A>G MANE Select	NP_066124.1:p.His661Arg
NM_020630.6:c.1982A>G	NP_065681.1:p.His661Arg