Canonical Allele Identifier: CA376557915

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43123769G>A , CM000672.2:g.43123769G>A	GRCh38
NC_000010.10:g.43619217G>A , CM000672.1:g.43619217G>A	GRCh37
NC_000010.9:g.42939223G>A	NCBI36
NG_007489.1:g.51701G>A , LRG_518:g.51701G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.2900G>A MANE Select	NP_066124.1:p.Gly967Asp
ENST00000355710.8:c.2900G>A MANE Select	ENSP00000347942.3:p.Gly967Asp
NM_001355216.1:c.2138G>A	NP_001342145.1:p.Gly713Asp
NM_020630.4:c.2900G>A , LRG_518t2:c.2900G>A	NP_065681.1:p.Gly967Asp
NM_020630.5:c.2900G>A	NP_065681.1:p.Gly967Asp
NM_020630.6:c.2900G>A	NP_065681.1:p.Gly967Asp
NM_020975.4:c.2900G>A , LRG_518t1:c.2900G>A	NP_066124.1:p.Gly967Asp
NM_020975.5:c.2900G>A	NP_066124.1:p.Gly967Asp
ENST00000340058.5:c.2900G>A	ENSP00000344798.4:p.Gly967Asp
ENST00000340058.6:c.2900G>A	ENSP00000344798.4:p.Gly967Asp
ENST00000355710.7:c.2900G>A	ENSP00000347942.3:p.Gly967Asp
ENST00000615310.4:c.*249G>A	ENSP00000480088.1:n.*249G>A
ENST00000615310.5:c.2504G>A	ENSP00000480088.2:p.Gly835Asp
ENST00000671844.1:c.*1494G>A	ENSP00000500541.1:n.*1494G>A
ENST00000672389.1:c.*1494G>A	ENSP00000500252.1:n.*1494G>A
ENST00000683007.1:n.2474G>A
XM_011540027.1:c.2900G>A	XP_011538329.1:p.Gly967Asp