Canonical Allele Identifier: CA2739265337

Gene: RET

Linked Data

• ClinVar Variation Id: 2918367
• ClinVar RCV Id: RCV003647216

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077340dup , CM000672.2:g.43077340dup	GRCh38
NC_000010.10:g.43572788dup , CM000672.1:g.43572788dup	GRCh37
NC_000010.9:g.42892794dup	NCBI36
NG_007489.1:g.5272dup , LRG_518:g.5272dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.73+9dup	ENSP00000480088.2:n.73+9dup
ENST00000340058.6:c.73+9dup	ENSP00000344798.4:n.73+9dup
ENST00000355710.8:c.73+9dup MANE Select	ENSP00000347942.3:n.73+9dup
ENST00000671844.1:c.73+9dup	ENSP00000500541.1:n.73+9dup
ENST00000672389.1:c.73+9dup	ENSP00000500252.1:n.73+9dup
ENST00000340058.5:c.73+9dup	ENSP00000344798.4:n.73+9dup
ENST00000355710.7:c.73+9dup	ENSP00000347942.3:n.73+9dup
ENST00000498820.5:c.73+9dup	ENSP00000419080.1:n.73+9dup
ENST00000615310.4:c.73+9dup	ENSP00000480088.1:n.73+9dup
NM_020630.4:c.73+9dup , LRG_518t2:c.73+9dup	NP_065681.1:n.73+9dup
NM_020975.4:c.73+9dup , LRG_518t1:c.73+9dup	NP_066124.1:n.73+9dup
XM_011540027.1:c.73+9dup	XP_011538329.1:n.73+9dup
NM_020630.5:c.73+9dup	NP_065681.1:n.73+9dup
NM_020975.5:c.73+9dup	NP_066124.1:n.73+9dup
NM_020975.6:c.73+9dup MANE Select	NP_066124.1:n.73+9dup
NM_020630.6:c.73+9dup	NP_065681.1:n.73+9dup