Canonical Allele Identifier: CA376545111

Gene: RET

Linked Data

• ClinVar Variation Id: 543748
• ClinVar RCV Id: RCV000654587 ; RCV002422431 ; RCV003465423
• dbSNP Id: rs1554817823
• gnomAD v4: 10-43105122-G-A
• MyVariant Identifiers: chr10:g.43600570G>A (hg19) ; chr10:g.43105122G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43105122G>A , CM000672.2:g.43105122G>A	GRCh38
NC_000010.10:g.43600570G>A , CM000672.1:g.43600570G>A	GRCh37
NC_000010.9:g.42920576G>A	NCBI36
NG_007489.1:g.33054G>A , LRG_518:g.33054G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.796G>A	ENSP00000480088.2:p.Asp266Asn
ENST00000683007.1:n.370G>A
ENST00000340058.6:c.796G>A	ENSP00000344798.4:p.Asp266Asn
ENST00000355710.8:c.796G>A MANE Select	ENSP00000347942.3:p.Asp266Asn
ENST00000671844.1:c.625+2493G>A	ENSP00000500541.1:n.625+2493G>A
ENST00000672389.1:c.74-6085G>A	ENSP00000500252.1:n.74-6085G>A
ENST00000340058.5:c.796G>A	ENSP00000344798.4:p.Asp266Asn
ENST00000355710.7:c.796G>A	ENSP00000347942.3:p.Asp266Asn
ENST00000479913.1:n.391G>A
ENST00000498820.5:c.74-6977G>A	ENSP00000419080.1:n.74-6977G>A
ENST00000615310.4:c.796G>A	ENSP00000480088.1:p.Asp266Asn
NM_020630.4:c.796G>A , LRG_518t2:c.796G>A	NP_065681.1:p.Asp266Asn
NM_020975.4:c.796G>A , LRG_518t1:c.796G>A	NP_066124.1:p.Asp266Asn
XM_011540027.1:c.796G>A	XP_011538329.1:p.Asp266Asn
NM_001355216.1:c.34G>A	NP_001342145.1:p.Asp12Asn
NM_020630.5:c.796G>A	NP_065681.1:p.Asp266Asn
NM_020975.5:c.796G>A	NP_066124.1:p.Asp266Asn
NM_020975.6:c.796G>A MANE Select	NP_066124.1:p.Asp266Asn
NM_020630.6:c.796G>A	NP_065681.1:p.Asp266Asn