Canonical Allele Identifier: CA009216

Gene: RET

Linked Data

• ClinVar Variation Id: 136117
• ClinVar RCV Id: RCV000123319 ; RCV001019149
• dbSNP Id: rs587780812
• gnomAD v2: 10-43572737-C-G
• gnomAD v4: 10-43077289-C-G
• MyVariant Identifiers: chr10:g.43572737C>G (hg19) ; chr10:g.43077289C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077289C>G , CM000672.2:g.43077289C>G	GRCh38
NC_000010.10:g.43572737C>G , CM000672.1:g.43572737C>G	GRCh37
NC_000010.9:g.42892743C>G	NCBI36
NG_007489.1:g.5221C>G , LRG_518:g.5221C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.31C>G	ENSP00000480088.2:p.Leu11Val
ENST00000340058.6:c.31C>G	ENSP00000344798.4:p.Leu11Val
ENST00000355710.8:c.31C>G MANE Select	ENSP00000347942.3:p.Leu11Val
ENST00000671844.1:c.31C>G	ENSP00000500541.1:p.Leu11Val
ENST00000672389.1:c.31C>G	ENSP00000500252.1:p.Leu11Val
ENST00000340058.5:c.31C>G	ENSP00000344798.4:p.Leu11Val
ENST00000355710.7:c.31C>G	ENSP00000347942.3:p.Leu11Val
ENST00000498820.5:c.31C>G	ENSP00000419080.1:p.Leu11Val
ENST00000615310.4:c.31C>G	ENSP00000480088.1:p.Leu11Val
NM_020630.4:c.31C>G , LRG_518t2:c.31C>G	NP_065681.1:p.Leu11Val
NM_020975.4:c.31C>G , LRG_518t1:c.31C>G	NP_066124.1:p.Leu11Val
XM_011540027.1:c.31C>G	XP_011538329.1:p.Leu11Val
NM_020630.5:c.31C>G	NP_065681.1:p.Leu11Val
NM_020975.5:c.31C>G	NP_066124.1:p.Leu11Val
NM_020975.6:c.31C>G MANE Select	NP_066124.1:p.Leu11Val
NM_020630.6:c.31C>G	NP_065681.1:p.Leu11Val