Canonical Allele Identifier: CA376553433

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114738T>G , CM000672.2:g.43114738T>G	GRCh38
NC_000010.10:g.43610186T>G , CM000672.1:g.43610186T>G	GRCh37
NC_000010.9:g.42930192T>G	NCBI36
NG_007489.1:g.42670T>G , LRG_518:g.42670T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.2136+2T>G MANE Select	NP_066124.1:n.2136+2T>G
ENST00000355710.8:c.2136+2T>G MANE Select	ENSP00000347942.3:n.2136+2T>G
NM_001355216.1:c.1374+2T>G	NP_001342145.1:n.1374+2T>G
NM_020630.4:c.2136+2T>G , LRG_518t2:c.2136+2T>G	NP_065681.1:n.2136+2T>G
NM_020630.5:c.2136+2T>G	NP_065681.1:n.2136+2T>G
NM_020630.6:c.2136+2T>G	NP_065681.1:n.2136+2T>G
NM_020975.4:c.2136+2T>G , LRG_518t1:c.2136+2T>G	NP_066124.1:n.2136+2T>G
NM_020975.5:c.2136+2T>G	NP_066124.1:n.2136+2T>G
ENST00000340058.5:c.2136+2T>G	ENSP00000344798.4:n.2136+2T>G
ENST00000340058.6:c.2136+2T>G	ENSP00000344798.4:n.2136+2T>G
ENST00000355710.7:c.2136+2T>G	ENSP00000347942.3:n.2136+2T>G
ENST00000615310.4:c.1289+3506T>G	ENSP00000480088.1:n.1289+3506T>G
ENST00000615310.5:c.1740+2T>G	ENSP00000480088.2:n.1740+2T>G
ENST00000671844.1:c.*730+2T>G	ENSP00000500541.1:n.*730+2T>G
ENST00000672389.1:c.*730+2T>G	ENSP00000500252.1:n.*730+2T>G
ENST00000683007.1:n.1710+2T>G
ENST00000683872.1:n.1701+2T>G
XM_011540027.1:c.2136+2T>G	XP_011538329.1:n.2136+2T>G