Canonical Allele Identifier: CA469028181

Gene: RET

Linked Data

• ClinVar Variation Id: 1790198
• ClinVar RCV Id: RCV002450132
• MyVariant Identifiers: chr10:g.43613900C>T (hg19) ; chr10:g.43118452C>T (hg38)
• PubMed: PMID:28647780

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118452C>T , CM000672.2:g.43118452C>T	GRCh38
NC_000010.10:g.43613900C>T , CM000672.1:g.43613900C>T	GRCh37
NC_000010.9:g.42933906C>T	NCBI36
NG_007489.1:g.46384C>T , LRG_518:g.46384C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1968C>T	ENSP00000480088.2:p.Ile656=
ENST00000683007.1:n.1938C>T
ENST00000683872.1:n.1929C>T
ENST00000340058.6:c.2364C>T	ENSP00000344798.4:p.Ile788=
ENST00000355710.8:c.2364C>T MANE Select	ENSP00000347942.3:p.Ile788=
ENST00000671844.1:c.*958C>T	ENSP00000500541.1:n.*958C>T
ENST00000672389.1:c.*958C>T	ENSP00000500252.1:n.*958C>T
ENST00000340058.5:c.2364C>T	ENSP00000344798.4:p.Ile788=
ENST00000355710.7:c.2364C>T	ENSP00000347942.3:p.Ile788=
ENST00000615310.4:c.1290-1250C>T	ENSP00000480088.1:n.1290-1250C>T
NM_020630.4:c.2364C>T , LRG_518t2:c.2364C>T	NP_065681.1:p.Ile788=
NM_020975.4:c.2364C>T , LRG_518t1:c.2364C>T	NP_066124.1:p.Ile788=
XM_011540027.1:c.2364C>T	XP_011538329.1:p.Ile788=
NM_001355216.1:c.1602C>T	NP_001342145.1:p.Ile534=
NM_020630.5:c.2364C>T	NP_065681.1:p.Ile788=
NM_020975.5:c.2364C>T	NP_066124.1:p.Ile788=
NM_020975.6:c.2364C>T MANE Select	NP_066124.1:p.Ile788=
NM_020630.6:c.2364C>T	NP_065681.1:p.Ile788=