Canonical Allele Identifier: CA10587083

Gene: RET

Linked Data

• ClinVar Variation Id: 261395
• ClinVar RCV Id: RCV000252880 ; RCV000572452 ; RCV000654622 ; RCV003316444
• dbSNP Id: rs886038663
• gnomAD v2: 10-43609956-G-A
• gnomAD v3: 10-43114508-G-A
• gnomAD v4: 10-43114508-G-A
• COSMIC: COSM1474612 ; COSM5214509
• MyVariant Identifiers: chr10:g.43609956G>A (hg19) ; chr10:g.43114508G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114508G>A , CM000672.2:g.43114508G>A	GRCh38
NC_000010.10:g.43609956G>A , CM000672.1:g.43609956G>A	GRCh37
NC_000010.9:g.42929962G>A	NCBI36
NG_007489.1:g.42440G>A , LRG_518:g.42440G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1512G>A	ENSP00000480088.2:p.Thr504=
ENST00000683007.1:n.1482G>A
ENST00000683872.1:n.1473G>A
ENST00000340058.6:c.1908G>A	ENSP00000344798.4:p.Thr636=
ENST00000355710.8:c.1908G>A MANE Select	ENSP00000347942.3:p.Thr636=
ENST00000671844.1:c.*502G>A	ENSP00000500541.1:n.*502G>A
ENST00000672389.1:c.*502G>A	ENSP00000500252.1:n.*502G>A
ENST00000340058.5:c.1908G>A	ENSP00000344798.4:p.Thr636=
ENST00000355710.7:c.1908G>A	ENSP00000347942.3:p.Thr636=
ENST00000498820.5:c.459G>A	ENSP00000419080.1:p.Thr153=
ENST00000615310.4:c.1289+3276G>A	ENSP00000480088.1:n.1289+3276G>A
NM_020630.4:c.1908G>A , LRG_518t2:c.1908G>A	NP_065681.1:p.Thr636=
NM_020975.4:c.1908G>A , LRG_518t1:c.1908G>A	NP_066124.1:p.Thr636=
XM_011540027.1:c.1908G>A	XP_011538329.1:p.Thr636=
NM_001355216.1:c.1146G>A	NP_001342145.1:p.Thr382=
NM_020630.5:c.1908G>A	NP_065681.1:p.Thr636=
NM_020975.5:c.1908G>A	NP_066124.1:p.Thr636=
NM_020975.6:c.1908G>A MANE Select	NP_066124.1:p.Thr636=
NM_020630.6:c.1908G>A	NP_065681.1:p.Thr636=