Canonical Allele Identifier: CA206268552

Gene: RET

Linked Data

• dbSNP Id: rs188882445
• gnomAD v3: 10-43130175-C-T
• gnomAD v4: 10-43130175-C-T
• MyVariant Identifiers: chr10:g.43625623C>T (hg19) ; chr10:g.43130175C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130175C>T , CM000672.2:g.43130175C>T	GRCh38
NC_000010.10:g.43625623C>T , CM000672.1:g.43625623C>T	GRCh37
NC_000010.9:g.42945629C>T	NCBI36
NG_007489.1:g.58107C>T , LRG_518:g.58107C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*3421C>T	ENSP00000480088.2:n.*3421C>T
ENST00000683007.1:n.6214C>T
ENST00000355710.8:c.*1906C>T MANE Select	ENSP00000347942.3:n.*1906C>T
ENST00000355710.7:c.*1906C>T	ENSP00000347942.3:n.*1906C>T
ENST00000615310.4:c.*2600C>T	ENSP00000480088.1:n.*2600C>T
NM_020975.4:c.*1906C>T , LRG_518t1:c.*1906C>T	NP_066124.1:n.*1906C>T
XM_011540027.1:c.*674C>T	XP_011538329.1:n.*674C>T
NM_020975.5:c.*1906C>T	NP_066124.1:n.*1906C>T
NM_020975.6:c.*1906C>T MANE Select	NP_066124.1:n.*1906C>T