Canonical Allele Identifier: CA376556414

Gene: RET

Linked Data

• ClinVar Variation Id: 2870666
• ClinVar RCV Id: RCV003646768
• MyVariant Identifiers: chr10:g.43615095T>G (hg19) ; chr10:g.43119647T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119647T>G , CM000672.2:g.43119647T>G	GRCh38
NC_000010.10:g.43615095T>G , CM000672.1:g.43615095T>G	GRCh37
NC_000010.9:g.42935101T>G	NCBI36
NG_007489.1:g.47579T>G , LRG_518:g.47579T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2113T>G	ENSP00000480088.2:p.Ser705Ala
ENST00000683007.1:n.2083T>G
ENST00000683872.1:n.2074T>G
ENST00000340058.6:c.2509T>G	ENSP00000344798.4:p.Ser837Ala
ENST00000355710.8:c.2509T>G MANE Select	ENSP00000347942.3:p.Ser837Ala
ENST00000671844.1:c.*1103T>G	ENSP00000500541.1:n.*1103T>G
ENST00000672389.1:c.*1103T>G	ENSP00000500252.1:n.*1103T>G
ENST00000340058.5:c.2509T>G	ENSP00000344798.4:p.Ser837Ala
ENST00000355710.7:c.2509T>G	ENSP00000347942.3:p.Ser837Ala
ENST00000615310.4:c.1290-55T>G	ENSP00000480088.1:n.1290-55T>G
NM_020630.4:c.2509T>G , LRG_518t2:c.2509T>G	NP_065681.1:p.Ser837Ala
NM_020975.4:c.2509T>G , LRG_518t1:c.2509T>G	NP_066124.1:p.Ser837Ala
XM_011540027.1:c.2509T>G	XP_011538329.1:p.Ser837Ala
NM_001355216.1:c.1747T>G	NP_001342145.1:p.Ser583Ala
NM_020630.5:c.2509T>G	NP_065681.1:p.Ser837Ala
NM_020975.5:c.2509T>G	NP_066124.1:p.Ser837Ala
NM_020975.6:c.2509T>G MANE Select	NP_066124.1:p.Ser837Ala
NM_020630.6:c.2509T>G	NP_065681.1:p.Ser837Ala