Canonical Allele Identifier: CA2580081463

Gene: RET

Linked Data

• ClinVar Variation Id: 2025097
• ClinVar RCV Id: RCV002848185

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114501_43114502delinsTT , CM000672.2:g.43114501_43114502delinsTT	GRCh38
NC_000010.10:g.43609949_43609950delinsTT , CM000672.1:g.43609949_43609950delinsTT	GRCh37
NC_000010.9:g.42929955_42929956delinsTT	NCBI36
NG_007489.1:g.42433_42434delinsTT , LRG_518:g.42433_42434delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1505_1506delinsTT	ENSP00000480088.2:p.Cys502Phe
ENST00000683007.1:n.1475_1476delinsTT
ENST00000683872.1:n.1466_1467delinsTT
ENST00000340058.6:c.1901_1902delinsTT	ENSP00000344798.4:p.Cys634Phe
ENST00000355710.8:c.1901_1902delinsTT MANE Select	ENSP00000347942.3:p.Cys634Phe
ENST00000671844.1:c.*495_*496delinsTT	ENSP00000500541.1:n.*495_*496delinsTT
ENST00000672389.1:c.*495_*496delinsTT	ENSP00000500252.1:n.*495_*496delinsTT
ENST00000340058.5:c.1901_1902delinsTT	ENSP00000344798.4:p.Cys634Phe
ENST00000355710.7:c.1901_1902delinsTT	ENSP00000347942.3:p.Cys634Phe
ENST00000498820.5:c.452_453delinsTT	ENSP00000419080.1:p.Cys151Phe
ENST00000615310.4:c.1289+3269_1289+3270delinsTT	ENSP00000480088.1:n.1289+3269_1289+3270delinsTT
NM_020630.4:c.1901_1902delinsTT , LRG_518t2:c.1901_1902delinsTT	NP_065681.1:p.Cys634Phe
NM_020975.4:c.1901_1902delinsTT , LRG_518t1:c.1901_1902delinsTT	NP_066124.1:p.Cys634Phe
XM_011540027.1:c.1901_1902delinsTT	XP_011538329.1:p.Cys634Phe
NM_001355216.1:c.1139_1140delinsTT	NP_001342145.1:p.Cys380Phe
NM_020630.5:c.1901_1902delinsTT	NP_065681.1:p.Cys634Phe
NM_020975.5:c.1901_1902delinsTT	NP_066124.1:p.Cys634Phe
NM_020975.6:c.1901_1902delinsTT MANE Select	NP_066124.1:p.Cys634Phe
NM_020630.6:c.1901_1902delinsTT	NP_065681.1:p.Cys634Phe