Canonical Allele Identifier: CA376768005

Gene: RET

Linked Data

• ClinVar Variation Id: 584566
• ClinVar RCV Id: RCV000708761 ; RCV001213441
• dbSNP Id: rs1564480827
• gnomAD v4: 10-43077265-A-G
• MyVariant Identifiers: chr10:g.43572713A>G (hg19) ; chr10:g.43077265A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077265A>G , CM000672.2:g.43077265A>G	GRCh38
NC_000010.10:g.43572713A>G , CM000672.1:g.43572713A>G	GRCh37
NC_000010.9:g.42892719A>G	NCBI36
NG_007489.1:g.5197A>G , LRG_518:g.5197A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.7A>G	ENSP00000480088.2:p.Lys3Glu
ENST00000340058.6:c.7A>G	ENSP00000344798.4:p.Lys3Glu
ENST00000355710.8:c.7A>G MANE Select	ENSP00000347942.3:p.Lys3Glu
ENST00000671844.1:c.7A>G	ENSP00000500541.1:p.Lys3Glu
ENST00000672389.1:c.7A>G	ENSP00000500252.1:p.Lys3Glu
ENST00000340058.5:c.7A>G	ENSP00000344798.4:p.Lys3Glu
ENST00000355710.7:c.7A>G	ENSP00000347942.3:p.Lys3Glu
ENST00000498820.5:c.7A>G	ENSP00000419080.1:p.Lys3Glu
ENST00000615310.4:c.7A>G	ENSP00000480088.1:p.Lys3Glu
NM_020630.4:c.7A>G , LRG_518t2:c.7A>G	NP_065681.1:p.Lys3Glu
NM_020975.4:c.7A>G , LRG_518t1:c.7A>G	NP_066124.1:p.Lys3Glu
XM_011540027.1:c.7A>G	XP_011538329.1:p.Lys3Glu
NM_020630.5:c.7A>G	NP_065681.1:p.Lys3Glu
NM_020975.5:c.7A>G	NP_066124.1:p.Lys3Glu
NM_020975.6:c.7A>G MANE Select	NP_066124.1:p.Lys3Glu
NM_020630.6:c.7A>G	NP_065681.1:p.Lys3Glu