Canonical Allele Identifier: CA376555681

Gene: RET

Linked Data

• ClinVar Variation Id: 2000804
• ClinVar RCV Id: RCV002810652
• dbSNP Id: rs2132929413
• MyVariant Identifiers: chr10:g.43613863T>A (hg19) ; chr10:g.43118415T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118415T>A , CM000672.2:g.43118415T>A	GRCh38
NC_000010.10:g.43613863T>A , CM000672.1:g.43613863T>A	GRCh37
NC_000010.9:g.42933869T>A	NCBI36
NG_007489.1:g.46347T>A , LRG_518:g.46347T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1931T>A	ENSP00000480088.2:p.Phe644Tyr
ENST00000683007.1:n.1901T>A
ENST00000683872.1:n.1892T>A
ENST00000340058.6:c.2327T>A	ENSP00000344798.4:p.Phe776Tyr
ENST00000355710.8:c.2327T>A MANE Select	ENSP00000347942.3:p.Phe776Tyr
ENST00000671844.1:c.*921T>A	ENSP00000500541.1:n.*921T>A
ENST00000672389.1:c.*921T>A	ENSP00000500252.1:n.*921T>A
ENST00000340058.5:c.2327T>A	ENSP00000344798.4:p.Phe776Tyr
ENST00000355710.7:c.2327T>A	ENSP00000347942.3:p.Phe776Tyr
ENST00000615310.4:c.1290-1287T>A	ENSP00000480088.1:n.1290-1287T>A
NM_020630.4:c.2327T>A , LRG_518t2:c.2327T>A	NP_065681.1:p.Phe776Tyr
NM_020975.4:c.2327T>A , LRG_518t1:c.2327T>A	NP_066124.1:p.Phe776Tyr
XM_011540027.1:c.2327T>A	XP_011538329.1:p.Phe776Tyr
NM_001355216.1:c.1565T>A	NP_001342145.1:p.Phe522Tyr
NM_020630.5:c.2327T>A	NP_065681.1:p.Phe776Tyr
NM_020975.5:c.2327T>A	NP_066124.1:p.Phe776Tyr
NM_020975.6:c.2327T>A MANE Select	NP_066124.1:p.Phe776Tyr
NM_020630.6:c.2327T>A	NP_065681.1:p.Phe776Tyr