Canonical Allele Identifier: CA376552935

Gene: RET

Linked Data

• dbSNP Id: rs2132845622
• MyVariant Identifiers: chr10:g.43609964C>G (hg19) ; chr10:g.43114516C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114516C>G , CM000672.2:g.43114516C>G	GRCh38
NC_000010.10:g.43609964C>G , CM000672.1:g.43609964C>G	GRCh37
NC_000010.9:g.42929970C>G	NCBI36
NG_007489.1:g.42448C>G , LRG_518:g.42448C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1520C>G	ENSP00000480088.2:p.Ala507Gly
ENST00000683007.1:n.1490C>G
ENST00000683872.1:n.1481C>G
ENST00000340058.6:c.1916C>G	ENSP00000344798.4:p.Ala639Gly
ENST00000355710.8:c.1916C>G MANE Select	ENSP00000347942.3:p.Ala639Gly
ENST00000671844.1:c.*510C>G	ENSP00000500541.1:n.*510C>G
ENST00000672389.1:c.*510C>G	ENSP00000500252.1:n.*510C>G
ENST00000340058.5:c.1916C>G	ENSP00000344798.4:p.Ala639Gly
ENST00000355710.7:c.1916C>G	ENSP00000347942.3:p.Ala639Gly
ENST00000498820.5:c.467C>G	ENSP00000419080.1:p.Ala156Gly
ENST00000615310.4:c.1289+3284C>G	ENSP00000480088.1:n.1289+3284C>G
NM_020630.4:c.1916C>G , LRG_518t2:c.1916C>G	NP_065681.1:p.Ala639Gly
NM_020975.4:c.1916C>G , LRG_518t1:c.1916C>G	NP_066124.1:p.Ala639Gly
XM_011540027.1:c.1916C>G	XP_011538329.1:p.Ala639Gly
NM_001355216.1:c.1154C>G	NP_001342145.1:p.Ala385Gly
NM_020630.5:c.1916C>G	NP_065681.1:p.Ala639Gly
NM_020975.5:c.1916C>G	NP_066124.1:p.Ala639Gly
NM_020975.6:c.1916C>G MANE Select	NP_066124.1:p.Ala639Gly
NM_020630.6:c.1916C>G	NP_065681.1:p.Ala639Gly