Canonical Allele Identifier: CA009020

Gene: RET

Linked Data

• ClinVar Variation Id: 24962
• ClinVar RCV Id: RCV001851991 ; RCV002468975
• dbSNP Id: rs267607011
• gnomAD v4: 10-43120184-C-G
• MyVariant Identifiers: chr10:g.43615632C>G (hg19) ; chr10:g.43120184C>G (hg38)
• PubMed: PMID:11788682 ; PMID:17895320

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120184C>G , CM000672.2:g.43120184C>G	GRCh38
NC_000010.10:g.43615632C>G , CM000672.1:g.43615632C>G	GRCh37
NC_000010.9:g.42935638C>G	NCBI36
NG_007489.1:g.48116C>G , LRG_518:g.48116C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2315C>G	ENSP00000480088.2:p.Ser772Cys
ENST00000683007.1:n.2285C>G
ENST00000683872.1:n.2276C>G
ENST00000340058.6:c.2711C>G	ENSP00000344798.4:p.Ser904Cys
ENST00000355710.8:c.2711C>G MANE Select	ENSP00000347942.3:p.Ser904Cys
ENST00000671844.1:c.*1305C>G	ENSP00000500541.1:n.*1305C>G
ENST00000672389.1:c.*1305C>G	ENSP00000500252.1:n.*1305C>G
ENST00000340058.5:c.2711C>G	ENSP00000344798.4:p.Ser904Cys
ENST00000355710.7:c.2711C>G	ENSP00000347942.3:p.Ser904Cys
ENST00000615310.4:c.*60C>G	ENSP00000480088.1:n.*60C>G
NM_020630.4:c.2711C>G , LRG_518t2:c.2711C>G	NP_065681.1:p.Ser904Cys
NM_020975.4:c.2711C>G , LRG_518t1:c.2711C>G	NP_066124.1:p.Ser904Cys
XM_011540027.1:c.2711C>G	XP_011538329.1:p.Ser904Cys
NM_001355216.1:c.1949C>G	NP_001342145.1:p.Ser650Cys
NM_020630.5:c.2711C>G	NP_065681.1:p.Ser904Cys
NM_020975.5:c.2711C>G	NP_066124.1:p.Ser904Cys
NM_020975.6:c.2711C>G MANE Select	NP_066124.1:p.Ser904Cys
NM_020630.6:c.2711C>G	NP_065681.1:p.Ser904Cys