Canonical Allele Identifier: CA206268566

Gene: RET

Linked Data

• dbSNP Id: rs865786570
• MyVariant Identifiers: chr10:g.43625737C>T (hg19) ; chr10:g.43130289C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130289C>T , CM000672.2:g.43130289C>T	GRCh38
NC_000010.10:g.43625737C>T , CM000672.1:g.43625737C>T	GRCh37
NC_000010.9:g.42945743C>T	NCBI36
NG_007489.1:g.58221C>T , LRG_518:g.58221C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355710.8:c.*2020C>T MANE Select	ENSP00000347942.3:n.*2020C>T
ENST00000355710.7:c.*2020C>T	ENSP00000347942.3:n.*2020C>T
ENST00000615310.4:c.*2714C>T	ENSP00000480088.1:n.*2714C>T
NM_020975.4:c.*2020C>T , LRG_518t1:c.*2020C>T	NP_066124.1:n.*2020C>T
XM_011540027.1:c.*788C>T	XP_011538329.1:n.*788C>T
NM_020975.5:c.*2020C>T	NP_066124.1:n.*2020C>T
NM_020975.6:c.*2020C>T MANE Select	NP_066124.1:n.*2020C>T