Canonical Allele Identifier: CA376555754

Gene: RET

Linked Data

• ClinVar Variation Id: 1413815
• ClinVar RCV Id: RCV001928330
• dbSNP Id: rs1838124605
• MyVariant Identifiers: chr10:g.43613880G>A (hg19) ; chr10:g.43118432G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118432G>A , CM000672.2:g.43118432G>A	GRCh38
NC_000010.10:g.43613880G>A , CM000672.1:g.43613880G>A	GRCh37
NC_000010.9:g.42933886G>A	NCBI36
NG_007489.1:g.46364G>A , LRG_518:g.46364G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1948G>A	ENSP00000480088.2:p.Val650Ile
ENST00000683007.1:n.1918G>A
ENST00000683872.1:n.1909G>A
ENST00000340058.6:c.2344G>A	ENSP00000344798.4:p.Val782Ile
ENST00000355710.8:c.2344G>A MANE Select	ENSP00000347942.3:p.Val782Ile
ENST00000671844.1:c.*938G>A	ENSP00000500541.1:n.*938G>A
ENST00000672389.1:c.*938G>A	ENSP00000500252.1:n.*938G>A
ENST00000340058.5:c.2344G>A	ENSP00000344798.4:p.Val782Ile
ENST00000355710.7:c.2344G>A	ENSP00000347942.3:p.Val782Ile
ENST00000615310.4:c.1290-1270G>A	ENSP00000480088.1:n.1290-1270G>A
NM_020630.4:c.2344G>A , LRG_518t2:c.2344G>A	NP_065681.1:p.Val782Ile
NM_020975.4:c.2344G>A , LRG_518t1:c.2344G>A	NP_066124.1:p.Val782Ile
XM_011540027.1:c.2344G>A	XP_011538329.1:p.Val782Ile
NM_001355216.1:c.1582G>A	NP_001342145.1:p.Val528Ile
NM_020630.5:c.2344G>A	NP_065681.1:p.Val782Ile
NM_020975.5:c.2344G>A	NP_066124.1:p.Val782Ile
NM_020975.6:c.2344G>A MANE Select	NP_066124.1:p.Val782Ile
NM_020630.6:c.2344G>A	NP_065681.1:p.Val782Ile