Canonical Allele Identifier: CA376557154

Gene: RET

Linked Data

• dbSNP Id: rs2132960657
• MyVariant Identifiers: chr10:g.43615573G>C (hg19) ; chr10:g.43120125G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120125G>C , CM000672.2:g.43120125G>C	GRCh38
NC_000010.10:g.43615573G>C , CM000672.1:g.43615573G>C	GRCh37
NC_000010.9:g.42935579G>C	NCBI36
NG_007489.1:g.48057G>C , LRG_518:g.48057G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2256G>C	ENSP00000480088.2:p.Glu752Asp
ENST00000683007.1:n.2226G>C
ENST00000683872.1:n.2217G>C
ENST00000340058.6:c.2652G>C	ENSP00000344798.4:p.Glu884Asp
ENST00000355710.8:c.2652G>C MANE Select	ENSP00000347942.3:p.Glu884Asp
ENST00000671844.1:c.*1246G>C	ENSP00000500541.1:n.*1246G>C
ENST00000672389.1:c.*1246G>C	ENSP00000500252.1:n.*1246G>C
ENST00000340058.5:c.2652G>C	ENSP00000344798.4:p.Glu884Asp
ENST00000355710.7:c.2652G>C	ENSP00000347942.3:p.Glu884Asp
ENST00000615310.4:c.*1G>C	ENSP00000480088.1:n.*1G>C
NM_020630.4:c.2652G>C , LRG_518t2:c.2652G>C	NP_065681.1:p.Glu884Asp
NM_020975.4:c.2652G>C , LRG_518t1:c.2652G>C	NP_066124.1:p.Glu884Asp
XM_011540027.1:c.2652G>C	XP_011538329.1:p.Glu884Asp
NM_001355216.1:c.1890G>C	NP_001342145.1:p.Glu630Asp
NM_020630.5:c.2652G>C	NP_065681.1:p.Glu884Asp
NM_020975.5:c.2652G>C	NP_066124.1:p.Glu884Asp
NM_020975.6:c.2652G>C MANE Select	NP_066124.1:p.Glu884Asp
NM_020630.6:c.2652G>C	NP_065681.1:p.Glu884Asp