Canonical Allele Identifier: CA376552987

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114542G>T , CM000672.2:g.43114542G>T	GRCh38
NC_000010.10:g.43609990G>T , CM000672.1:g.43609990G>T	GRCh37
NC_000010.9:g.42929996G>T	NCBI36
NG_007489.1:g.42474G>T , LRG_518:g.42474G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1546G>T	ENSP00000480088.2:p.Val516Phe
ENST00000683007.1:n.1516G>T
ENST00000683872.1:n.1507G>T
ENST00000340058.6:c.1942G>T	ENSP00000344798.4:p.Val648Phe
ENST00000355710.8:c.1942G>T MANE Select	ENSP00000347942.3:p.Val648Phe
ENST00000671844.1:c.*536G>T	ENSP00000500541.1:n.*536G>T
ENST00000672389.1:c.*536G>T	ENSP00000500252.1:n.*536G>T
ENST00000340058.5:c.1942G>T	ENSP00000344798.4:p.Val648Phe
ENST00000355710.7:c.1942G>T	ENSP00000347942.3:p.Val648Phe
ENST00000498820.5:c.493G>T	ENSP00000419080.1:p.Val165Phe
ENST00000615310.4:c.1289+3310G>T	ENSP00000480088.1:n.1289+3310G>T
NM_020630.4:c.1942G>T , LRG_518t2:c.1942G>T	NP_065681.1:p.Val648Phe
NM_020975.4:c.1942G>T , LRG_518t1:c.1942G>T	NP_066124.1:p.Val648Phe
XM_011540027.1:c.1942G>T	XP_011538329.1:p.Val648Phe
NM_001355216.1:c.1180G>T	NP_001342145.1:p.Val394Phe
NM_020630.5:c.1942G>T	NP_065681.1:p.Val648Phe
NM_020975.5:c.1942G>T	NP_066124.1:p.Val648Phe
NM_020975.6:c.1942G>T MANE Select	NP_066124.1:p.Val648Phe
NM_020630.6:c.1942G>T	NP_065681.1:p.Val648Phe