Canonical Allele Identifier: CA009058

Gene: RET

Linked Data

• ClinVar Variation Id: 3227539
• ClinVar RCV Id: RCV004524657
• dbSNP Id: rs78347871
• COSMIC: COSM3437793 ; COSM3437794
• MyVariant Identifiers: chr10:g.43617398G>A (hg19) ; chr10:g.43121950G>A (hg38)
• PubMed: PMID:11955539

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43121950G>A , CM000672.2:g.43121950G>A	GRCh38
NC_000010.10:g.43617398G>A , CM000672.1:g.43617398G>A	GRCh37
NC_000010.9:g.42937404G>A	NCBI36
NG_007489.1:g.49882G>A , LRG_518:g.49882G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2339G>A	ENSP00000480088.2:p.Arg780Gln
ENST00000683007.1:n.2309G>A
ENST00000340058.6:c.2735G>A	ENSP00000344798.4:p.Arg912Gln
ENST00000355710.8:c.2735G>A MANE Select	ENSP00000347942.3:p.Arg912Gln
ENST00000671844.1:c.*1329G>A	ENSP00000500541.1:n.*1329G>A
ENST00000672389.1:c.*1329G>A	ENSP00000500252.1:n.*1329G>A
ENST00000340058.5:c.2735G>A	ENSP00000344798.4:p.Arg912Gln
ENST00000355710.7:c.2735G>A	ENSP00000347942.3:p.Arg912Gln
ENST00000615310.4:c.*84G>A	ENSP00000480088.1:n.*84G>A
NM_020630.4:c.2735G>A , LRG_518t2:c.2735G>A	NP_065681.1:p.Arg912Gln
NM_020975.4:c.2735G>A , LRG_518t1:c.2735G>A	NP_066124.1:p.Arg912Gln
XM_011540027.1:c.2735G>A	XP_011538329.1:p.Arg912Gln
NM_001355216.1:c.1973G>A	NP_001342145.1:p.Arg658Gln
NM_020630.5:c.2735G>A	NP_065681.1:p.Arg912Gln
NM_020975.5:c.2735G>A	NP_066124.1:p.Arg912Gln
NM_020975.6:c.2735G>A MANE Select	NP_066124.1:p.Arg912Gln
NM_020630.6:c.2735G>A	NP_065681.1:p.Arg912Gln