Canonical Allele Identifier: CA469028169

Gene: RET

Linked Data

• ClinVar Variation Id: 1096642
• ClinVar RCV Id: RCV001417946 ; RCV002449136
• dbSNP Id: rs1160720188
• gnomAD v2: 10-43613885-C-T
• gnomAD v3: 10-43118437-C-T
• gnomAD v4: 10-43118437-C-T
• MyVariant Identifiers: chr10:g.43613885C>T (hg19) ; chr10:g.43118437C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118437C>T , CM000672.2:g.43118437C>T	GRCh38
NC_000010.10:g.43613885C>T , CM000672.1:g.43613885C>T	GRCh37
NC_000010.9:g.42933891C>T	NCBI36
NG_007489.1:g.46369C>T , LRG_518:g.46369C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1953C>T	ENSP00000480088.2:p.Asn651=
ENST00000683007.1:n.1923C>T
ENST00000683872.1:n.1914C>T
ENST00000340058.6:c.2349C>T	ENSP00000344798.4:p.Asn783=
ENST00000355710.8:c.2349C>T MANE Select	ENSP00000347942.3:p.Asn783=
ENST00000671844.1:c.*943C>T	ENSP00000500541.1:n.*943C>T
ENST00000672389.1:c.*943C>T	ENSP00000500252.1:n.*943C>T
ENST00000340058.5:c.2349C>T	ENSP00000344798.4:p.Asn783=
ENST00000355710.7:c.2349C>T	ENSP00000347942.3:p.Asn783=
ENST00000615310.4:c.1290-1265C>T	ENSP00000480088.1:n.1290-1265C>T
NM_020630.4:c.2349C>T , LRG_518t2:c.2349C>T	NP_065681.1:p.Asn783=
NM_020975.4:c.2349C>T , LRG_518t1:c.2349C>T	NP_066124.1:p.Asn783=
XM_011540027.1:c.2349C>T	XP_011538329.1:p.Asn783=
NM_001355216.1:c.1587C>T	NP_001342145.1:p.Asn529=
NM_020630.5:c.2349C>T	NP_065681.1:p.Asn783=
NM_020975.5:c.2349C>T	NP_066124.1:p.Asn783=
NM_020975.6:c.2349C>T MANE Select	NP_066124.1:p.Asn783=
NM_020630.6:c.2349C>T	NP_065681.1:p.Asn783=