Canonical Allele Identifier: CA469479961

Gene: RET

Linked Data

• ClinVar Variation Id: 1377800
• ClinVar RCV Id: RCV001880840
• dbSNP Id: rs1414025702
• MyVariant Identifiers: chr10:g.43610124C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114676C>G , CM000672.2:g.43114676C>G	GRCh38
NC_000010.10:g.43610124C>G , CM000672.1:g.43610124C>G	GRCh37
NC_000010.9:g.42930130C>G	NCBI36
NG_007489.1:g.42608C>G , LRG_518:g.42608C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1680C>G	ENSP00000480088.2:p.Ala560=
ENST00000683007.1:n.1650C>G
ENST00000683872.1:n.1641C>G
ENST00000340058.6:c.2076C>G	ENSP00000344798.4:p.Ala692=
ENST00000355710.8:c.2076C>G MANE Select	ENSP00000347942.3:p.Ala692=
ENST00000671844.1:c.*670C>G	ENSP00000500541.1:n.*670C>G
ENST00000672389.1:c.*670C>G	ENSP00000500252.1:n.*670C>G
ENST00000340058.5:c.2076C>G	ENSP00000344798.4:p.Ala692=
ENST00000355710.7:c.2076C>G	ENSP00000347942.3:p.Ala692=
ENST00000615310.4:c.1289+3444C>G	ENSP00000480088.1:n.1289+3444C>G
NM_020630.4:c.2076C>G , LRG_518t2:c.2076C>G	NP_065681.1:p.Ala692=
NM_020975.4:c.2076C>G , LRG_518t1:c.2076C>G	NP_066124.1:p.Ala692=
XM_011540027.1:c.2076C>G	XP_011538329.1:p.Ala692=
NM_001355216.1:c.1314C>G	NP_001342145.1:p.Ala438=
NM_020630.5:c.2076C>G	NP_065681.1:p.Ala692=
NM_020975.5:c.2076C>G	NP_066124.1:p.Ala692=
NM_020975.6:c.2076C>G MANE Select	NP_066124.1:p.Ala692=
NM_020630.6:c.2076C>G	NP_065681.1:p.Ala692=