Canonical Allele Identifier: CA376545731

Gene: RET

Linked Data

• ClinVar Variation Id: 1366196
• ClinVar RCV Id: RCV001930060
• dbSNP Id: rs1837776769
• gnomAD v3: 10-43106403-T-G
• gnomAD v4: 10-43106403-T-G
• MyVariant Identifiers: chr10:g.43601851T>G (hg19) ; chr10:g.43106403T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106403T>G , CM000672.2:g.43106403T>G	GRCh38
NC_000010.10:g.43601851T>G , CM000672.1:g.43601851T>G	GRCh37
NC_000010.9:g.42921857T>G	NCBI36
NG_007489.1:g.34335T>G , LRG_518:g.34335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.867+1210T>G	ENSP00000480088.2:n.867+1210T>G
ENST00000683007.1:n.469T>G
ENST00000340058.6:c.895T>G	ENSP00000344798.4:p.Phe299Val
ENST00000355710.8:c.895T>G MANE Select	ENSP00000347942.3:p.Phe299Val
ENST00000671844.1:c.625+3774T>G	ENSP00000500541.1:n.625+3774T>G
ENST00000672389.1:c.74-4804T>G	ENSP00000500252.1:n.74-4804T>G
ENST00000340058.5:c.895T>G	ENSP00000344798.4:p.Phe299Val
ENST00000355710.7:c.895T>G	ENSP00000347942.3:p.Phe299Val
ENST00000479913.1:n.490T>G
ENST00000498820.5:c.74-5696T>G	ENSP00000419080.1:n.74-5696T>G
ENST00000615310.4:c.895T>G	ENSP00000480088.1:p.Phe299Val
NM_020630.4:c.895T>G , LRG_518t2:c.895T>G	NP_065681.1:p.Phe299Val
NM_020975.4:c.895T>G , LRG_518t1:c.895T>G	NP_066124.1:p.Phe299Val
XM_011540027.1:c.895T>G	XP_011538329.1:p.Phe299Val
NM_001355216.1:c.133T>G	NP_001342145.1:p.Phe45Val
NM_020630.5:c.895T>G	NP_065681.1:p.Phe299Val
NM_020975.5:c.895T>G	NP_066124.1:p.Phe299Val
NM_020975.6:c.895T>G MANE Select	NP_066124.1:p.Phe299Val
NM_020630.6:c.895T>G	NP_065681.1:p.Phe299Val