Canonical Allele Identifier: CA009051

Gene: RET

Linked Data

• ClinVar Variation Id: 1406187
• ClinVar RCV Id: RCV001906841
• dbSNP Id: rs377767431
• MyVariant Identifiers: chr10:g.43615641A>T (hg19) ; chr10:g.43120193A>T (hg38)
• PubMed: PMID:1 ; PMID:160 ; PMID:168 ; PMID:818 ; PMID:845 ; PMID:976 ; PMID:11688458

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120193A>T , CM000672.2:g.43120193A>T	GRCh38
NC_000010.10:g.43615641A>T , CM000672.1:g.43615641A>T	GRCh37
NC_000010.9:g.42935647A>T	NCBI36
NG_007489.1:g.48125A>T , LRG_518:g.48125A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2324A>T	ENSP00000480088.2:p.Lys775Met
ENST00000683007.1:n.2294A>T
ENST00000683872.1:n.2285A>T
ENST00000340058.6:c.2720A>T	ENSP00000344798.4:p.Lys907Met
ENST00000355710.8:c.2720A>T MANE Select	ENSP00000347942.3:p.Lys907Met
ENST00000671844.1:c.*1314A>T	ENSP00000500541.1:n.*1314A>T
ENST00000672389.1:c.*1314A>T	ENSP00000500252.1:n.*1314A>T
ENST00000340058.5:c.2720A>T	ENSP00000344798.4:p.Lys907Met
ENST00000355710.7:c.2720A>T	ENSP00000347942.3:p.Lys907Met
ENST00000615310.4:c.*69A>T	ENSP00000480088.1:n.*69A>T
NM_020630.4:c.2720A>T , LRG_518t2:c.2720A>T	NP_065681.1:p.Lys907Met
NM_020975.4:c.2720A>T , LRG_518t1:c.2720A>T	NP_066124.1:p.Lys907Met
XM_011540027.1:c.2720A>T	XP_011538329.1:p.Lys907Met
NM_001355216.1:c.1958A>T	NP_001342145.1:p.Lys653Met
NM_020630.5:c.2720A>T	NP_065681.1:p.Lys907Met
NM_020975.5:c.2720A>T	NP_066124.1:p.Lys907Met
NM_020975.6:c.2720A>T MANE Select	NP_066124.1:p.Lys907Met
NM_020630.6:c.2720A>T	NP_065681.1:p.Lys907Met