Canonical Allele Identifier: CA376558065

Gene: RET

Linked Data

• dbSNP Id: rs2133016304
• MyVariant Identifiers: chr10:g.43620351G>A (hg19) ; chr10:g.43124903G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43124903G>A , CM000672.2:g.43124903G>A	GRCh38
NC_000010.10:g.43620351G>A , CM000672.1:g.43620351G>A	GRCh37
NC_000010.9:g.42940357G>A	NCBI36
NG_007489.1:g.52835G>A , LRG_518:g.52835G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2564G>A	ENSP00000480088.2:p.Cys855Tyr
ENST00000683007.1:n.2534G>A
ENST00000340058.6:c.2960G>A	ENSP00000344798.4:p.Cys987Tyr
ENST00000355710.8:c.2960G>A MANE Select	ENSP00000347942.3:p.Cys987Tyr
ENST00000671844.1:c.*1554G>A	ENSP00000500541.1:n.*1554G>A
ENST00000672389.1:c.*1554G>A	ENSP00000500252.1:n.*1554G>A
ENST00000340058.5:c.2960G>A	ENSP00000344798.4:p.Cys987Tyr
ENST00000355710.7:c.2960G>A	ENSP00000347942.3:p.Cys987Tyr
ENST00000615310.4:c.*309G>A	ENSP00000480088.1:n.*309G>A
NM_020630.4:c.2960G>A , LRG_518t2:c.2960G>A	NP_065681.1:p.Cys987Tyr
NM_020975.4:c.2960G>A , LRG_518t1:c.2960G>A	NP_066124.1:p.Cys987Tyr
XM_011540027.1:c.2960G>A	XP_011538329.1:p.Cys987Tyr
NM_001355216.1:c.2198G>A	NP_001342145.1:p.Cys733Tyr
NM_020630.5:c.2960G>A	NP_065681.1:p.Cys987Tyr
NM_020975.5:c.2960G>A	NP_066124.1:p.Cys987Tyr
NM_020975.6:c.2960G>A MANE Select	NP_066124.1:p.Cys987Tyr
NM_020630.6:c.2960G>A	NP_065681.1:p.Cys987Tyr