Canonical Allele Identifier: CA469028186

Gene: RET

Linked Data

• ClinVar Variation Id: 1790226
• ClinVar RCV Id: RCV002457732
• COSMIC: COSM4925543 ; COSM4925544
• MyVariant Identifiers: chr10:g.43613903A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118455A>G , CM000672.2:g.43118455A>G	GRCh38
NC_000010.10:g.43613903A>G , CM000672.1:g.43613903A>G	GRCh37
NC_000010.9:g.42933909A>G	NCBI36
NG_007489.1:g.46387A>G , LRG_518:g.46387A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1971A>G	ENSP00000480088.2:p.Lys657=
ENST00000683007.1:n.1941A>G
ENST00000683872.1:n.1932A>G
ENST00000340058.6:c.2367A>G	ENSP00000344798.4:p.Lys789=
ENST00000355710.8:c.2367A>G MANE Select	ENSP00000347942.3:p.Lys789=
ENST00000671844.1:c.*961A>G	ENSP00000500541.1:n.*961A>G
ENST00000672389.1:c.*961A>G	ENSP00000500252.1:n.*961A>G
ENST00000340058.5:c.2367A>G	ENSP00000344798.4:p.Lys789=
ENST00000355710.7:c.2367A>G	ENSP00000347942.3:p.Lys789=
ENST00000615310.4:c.1290-1247A>G	ENSP00000480088.1:n.1290-1247A>G
NM_020630.4:c.2367A>G , LRG_518t2:c.2367A>G	NP_065681.1:p.Lys789=
NM_020975.4:c.2367A>G , LRG_518t1:c.2367A>G	NP_066124.1:p.Lys789=
XM_011540027.1:c.2367A>G	XP_011538329.1:p.Lys789=
NM_001355216.1:c.1605A>G	NP_001342145.1:p.Lys535=
NM_020630.5:c.2367A>G	NP_065681.1:p.Lys789=
NM_020975.5:c.2367A>G	NP_066124.1:p.Lys789=
NM_020975.6:c.2367A>G MANE Select	NP_066124.1:p.Lys789=
NM_020630.6:c.2367A>G	NP_065681.1:p.Lys789=