Canonical Allele Identifier: CA2695211984

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118481dup , CM000672.2:g.43118481dup	GRCh38
NC_000010.10:g.43613929dup , CM000672.1:g.43613929dup	GRCh37
NC_000010.9:g.42933935dup	NCBI36
NG_007489.1:g.46413dup , LRG_518:g.46413dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1996+1dup
ENST00000683007.1:n.1966+1dup
ENST00000683872.1:n.1957+1dup
ENST00000340058.6:c.2392+1dup
ENST00000355710.8:c.2392+1dup
ENST00000671844.1:c.*986+1dup
ENST00000672389.1:c.*986+1dup
ENST00000340058.5:c.2392+1dup
ENST00000355710.7:c.2392+1dup
ENST00000615310.4:c.1290-1221dup	ENSP00000480088.1:n.1290-1221dup
NM_020630.4:c.2392+1dup , LRG_518t2:c.2392+1dup
NM_020975.4:c.2392+1dup , LRG_518t1:c.2392+1dup
XM_011540027.1:c.2392+1dup
NM_001355216.1:c.1630+1dup
NM_020630.5:c.2392+1dup
NM_020975.5:c.2392+1dup
NM_020975.6:c.2392+1dup
NM_020630.6:c.2392+1dup