Canonical Allele Identifier: CA2721934369

Gene: RET

Linked Data

• dbSNP Id: rs2132932740

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118495A>G , CM000672.2:g.43118495A>G	GRCh38
NC_000010.10:g.43613943A>G , CM000672.1:g.43613943A>G	GRCh37
NC_000010.9:g.42933949A>G	NCBI36
NG_007489.1:g.46427A>G , LRG_518:g.46427A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1996+15A>G	ENSP00000480088.2:n.1996+15A>G
ENST00000683007.1:n.1966+15A>G
ENST00000683872.1:n.1957+15A>G
ENST00000340058.6:c.2392+15A>G	ENSP00000344798.4:n.2392+15A>G
ENST00000355710.8:c.2392+15A>G MANE Select	ENSP00000347942.3:n.2392+15A>G
ENST00000671844.1:c.*986+15A>G	ENSP00000500541.1:n.*986+15A>G
ENST00000672389.1:c.*986+15A>G	ENSP00000500252.1:n.*986+15A>G
ENST00000340058.5:c.2392+15A>G	ENSP00000344798.4:n.2392+15A>G
ENST00000355710.7:c.2392+15A>G	ENSP00000347942.3:n.2392+15A>G
ENST00000615310.4:c.1290-1207A>G	ENSP00000480088.1:n.1290-1207A>G
NM_020630.4:c.2392+15A>G , LRG_518t2:c.2392+15A>G	NP_065681.1:n.2392+15A>G
NM_020975.4:c.2392+15A>G , LRG_518t1:c.2392+15A>G	NP_066124.1:n.2392+15A>G
XM_011540027.1:c.2392+15A>G	XP_011538329.1:n.2392+15A>G
NM_001355216.1:c.1630+15A>G	NP_001342145.1:n.1630+15A>G
NM_020630.5:c.2392+15A>G	NP_065681.1:n.2392+15A>G
NM_020975.5:c.2392+15A>G	NP_066124.1:n.2392+15A>G
NM_020975.6:c.2392+15A>G MANE Select	NP_066124.1:n.2392+15A>G
NM_020630.6:c.2392+15A>G	NP_065681.1:n.2392+15A>G