Canonical Allele Identifier: CA376549682

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43111393A>G , CM000672.2:g.43111393A>G	GRCh38
NC_000010.10:g.43606841A>G , CM000672.1:g.43606841A>G	GRCh37
NC_000010.9:g.42926847A>G	NCBI36
NG_007489.1:g.39325A>G , LRG_518:g.39325A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1450A>G MANE Select	NP_066124.1:p.Met484Val
ENST00000355710.8:c.1450A>G MANE Select	ENSP00000347942.3:p.Met484Val
NM_001355216.1:c.688A>G	NP_001342145.1:p.Met230Val
NM_020630.4:c.1450A>G , LRG_518t2:c.1450A>G	NP_065681.1:p.Met484Val
NM_020630.5:c.1450A>G	NP_065681.1:p.Met484Val
NM_020630.6:c.1450A>G	NP_065681.1:p.Met484Val
NM_020975.4:c.1450A>G , LRG_518t1:c.1450A>G	NP_066124.1:p.Met484Val
NM_020975.5:c.1450A>G	NP_066124.1:p.Met484Val
ENST00000340058.5:c.1450A>G	ENSP00000344798.4:p.Met484Val
ENST00000340058.6:c.1450A>G	ENSP00000344798.4:p.Met484Val
ENST00000355710.7:c.1450A>G	ENSP00000347942.3:p.Met484Val
ENST00000498820.5:c.74-706A>G	ENSP00000419080.1:n.74-706A>G
ENST00000615310.4:c.1289+161A>G	ENSP00000480088.1:n.1289+161A>G
ENST00000615310.5:c.1054A>G	ENSP00000480088.2:p.Met352Val
ENST00000671844.1:c.*44A>G	ENSP00000500541.1:n.*44A>G
ENST00000672389.1:c.*44A>G	ENSP00000500252.1:n.*44A>G
ENST00000683007.1:n.1024A>G
ENST00000683872.1:n.211A>G
XM_011540027.1:c.1450A>G	XP_011538329.1:p.Met484Val