Canonical Allele Identifier: CA2608894087

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077071T>G , CM000672.2:g.43077071T>G	GRCh38
NC_000010.10:g.43572519T>G , CM000672.1:g.43572519T>G	GRCh37
NC_000010.9:g.42892525T>G	NCBI36
NG_007489.1:g.5003T>G , LRG_518:g.5003T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340058.6:c.-188T>G	ENSP00000344798.4:n.-188T>G
ENST00000355710.8:c.-188T>G MANE Select	ENSP00000347942.3:n.-188T>G
ENST00000671844.1:c.-188T>G	ENSP00000500541.1:n.-188T>G
ENST00000672389.1:c.-188T>G	ENSP00000500252.1:n.-188T>G
ENST00000355710.7:c.-188T>G	ENSP00000347942.3:n.-188T>G
ENST00000615310.4:c.-188T>G	ENSP00000480088.1:n.-188T>G
NM_020630.4:c.-188T>G , LRG_518t2:c.-188T>G	NP_065681.1:n.-188T>G
NM_020975.4:c.-188T>G , LRG_518t1:c.-188T>G	NP_066124.1:n.-188T>G
XM_011540027.1:c.-188T>G	XP_011538329.1:n.-188T>G
NM_020630.5:c.-188T>G	NP_065681.1:n.-188T>G
NM_020975.5:c.-188T>G	NP_066124.1:n.-188T>G
NM_020975.6:c.-188T>G MANE Select	NP_066124.1:n.-188T>G
NM_020630.6:c.-188T>G	NP_065681.1:n.-188T>G