Canonical Allele Identifier: CA376550003

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43111450A>G , CM000672.2:g.43111450A>G	GRCh38
NC_000010.10:g.43606898A>G , CM000672.1:g.43606898A>G	GRCh37
NC_000010.9:g.42926904A>G	NCBI36
NG_007489.1:g.39382A>G , LRG_518:g.39382A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1507A>G MANE Select	NP_066124.1:p.Thr503Ala
ENST00000355710.8:c.1507A>G MANE Select	ENSP00000347942.3:p.Thr503Ala
NM_001355216.1:c.745A>G	NP_001342145.1:p.Thr249Ala
NM_020630.4:c.1507A>G , LRG_518t2:c.1507A>G	NP_065681.1:p.Thr503Ala
NM_020630.5:c.1507A>G	NP_065681.1:p.Thr503Ala
NM_020630.6:c.1507A>G	NP_065681.1:p.Thr503Ala
NM_020975.4:c.1507A>G , LRG_518t1:c.1507A>G	NP_066124.1:p.Thr503Ala
NM_020975.5:c.1507A>G	NP_066124.1:p.Thr503Ala
ENST00000340058.5:c.1507A>G	ENSP00000344798.4:p.Thr503Ala
ENST00000340058.6:c.1507A>G	ENSP00000344798.4:p.Thr503Ala
ENST00000355710.7:c.1507A>G	ENSP00000347942.3:p.Thr503Ala
ENST00000498820.5:c.74-649A>G	ENSP00000419080.1:n.74-649A>G
ENST00000615310.4:c.1289+218A>G	ENSP00000480088.1:n.1289+218A>G
ENST00000615310.5:c.1111A>G	ENSP00000480088.2:p.Thr371Ala
ENST00000671844.1:c.*101A>G	ENSP00000500541.1:n.*101A>G
ENST00000672389.1:c.*101A>G	ENSP00000500252.1:n.*101A>G
ENST00000683007.1:n.1081A>G
ENST00000683872.1:n.268A>G
XM_011540027.1:c.1507A>G	XP_011538329.1:p.Thr503Ala