Canonical Allele Identifier: CA008648

Gene: RET

Linked Data

• ClinVar Variation Id: 38611
• ClinVar RCV Id: RCV000032037 ; RCV000410061 ; RCV000411546 ; RCV002426530 ; RCV002307370
• dbSNP Id: rs78014899
• gnomAD v4: 10-43118392-G-T
• MyVariant Identifiers: chr10:g.43613840G>T (hg19) ; chr10:g.43118392G>T (hg38)
• PubMed: PMID:112 ; PMID:201 ; PMID:304 ; PMID:648 ; PMID:811 ; PMID:11230481 ; PMID:12016484 ; PMID:12116277 ; PMID:21934104

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118392G>T , CM000672.2:g.43118392G>T	GRCh38
NC_000010.10:g.43613840G>T , CM000672.1:g.43613840G>T	GRCh37
NC_000010.9:g.42933846G>T	NCBI36
NG_007489.1:g.46324G>T , LRG_518:g.46324G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1908G>T	ENSP00000480088.2:p.Glu636Asp
ENST00000683007.1:n.1878G>T
ENST00000683872.1:n.1869G>T
ENST00000340058.6:c.2304G>T	ENSP00000344798.4:p.Glu768Asp
ENST00000355710.8:c.2304G>T MANE Select	ENSP00000347942.3:p.Glu768Asp
ENST00000671844.1:c.*898G>T	ENSP00000500541.1:n.*898G>T
ENST00000672389.1:c.*898G>T	ENSP00000500252.1:n.*898G>T
ENST00000340058.5:c.2304G>T	ENSP00000344798.4:p.Glu768Asp
ENST00000355710.7:c.2304G>T	ENSP00000347942.3:p.Glu768Asp
ENST00000615310.4:c.1290-1310G>T	ENSP00000480088.1:n.1290-1310G>T
NM_020630.4:c.2304G>T , LRG_518t2:c.2304G>T	NP_065681.1:p.Glu768Asp
NM_020975.4:c.2304G>T , LRG_518t1:c.2304G>T	NP_066124.1:p.Glu768Asp
XM_011540027.1:c.2304G>T	XP_011538329.1:p.Glu768Asp
NM_001355216.1:c.1542G>T	NP_001342145.1:p.Glu514Asp
NM_020630.5:c.2304G>T	NP_065681.1:p.Glu768Asp
NM_020975.5:c.2304G>T	NP_066124.1:p.Glu768Asp
NM_020975.6:c.2304G>T MANE Select	NP_066124.1:p.Glu768Asp
NM_020630.6:c.2304G>T	NP_065681.1:p.Glu768Asp