Canonical Allele Identifier: CA376558069

Gene: RET

Linked Data

• MyVariant Identifiers: chr10:g.43620352C>G (hg19) ; chr10:g.43124904C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43124904C>G , CM000672.2:g.43124904C>G	GRCh38
NC_000010.10:g.43620352C>G , CM000672.1:g.43620352C>G	GRCh37
NC_000010.9:g.42940358C>G	NCBI36
NG_007489.1:g.52836C>G , LRG_518:g.52836C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2565C>G	ENSP00000480088.2:p.Cys855Trp
ENST00000683007.1:n.2535C>G
ENST00000340058.6:c.2961C>G	ENSP00000344798.4:p.Cys987Trp
ENST00000355710.8:c.2961C>G MANE Select	ENSP00000347942.3:p.Cys987Trp
ENST00000671844.1:c.*1555C>G	ENSP00000500541.1:n.*1555C>G
ENST00000672389.1:c.*1555C>G	ENSP00000500252.1:n.*1555C>G
ENST00000340058.5:c.2961C>G	ENSP00000344798.4:p.Cys987Trp
ENST00000355710.7:c.2961C>G	ENSP00000347942.3:p.Cys987Trp
ENST00000615310.4:c.*310C>G	ENSP00000480088.1:n.*310C>G
NM_020630.4:c.2961C>G , LRG_518t2:c.2961C>G	NP_065681.1:p.Cys987Trp
NM_020975.4:c.2961C>G , LRG_518t1:c.2961C>G	NP_066124.1:p.Cys987Trp
XM_011540027.1:c.2961C>G	XP_011538329.1:p.Cys987Trp
NM_001355216.1:c.2199C>G	NP_001342145.1:p.Cys733Trp
NM_020630.5:c.2961C>G	NP_065681.1:p.Cys987Trp
NM_020975.5:c.2961C>G	NP_066124.1:p.Cys987Trp
NM_020975.6:c.2961C>G MANE Select	NP_066124.1:p.Cys987Trp
NM_020630.6:c.2961C>G	NP_065681.1:p.Cys987Trp