Canonical Allele Identifier: CA469479981

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114689C>T , CM000672.2:g.43114689C>T	GRCh38
NC_000010.10:g.43610137C>T , CM000672.1:g.43610137C>T	GRCh37
NC_000010.9:g.42930143C>T	NCBI36
NG_007489.1:g.42621C>T , LRG_518:g.42621C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.2089C>T MANE Select	NP_066124.1:p.Leu697=
ENST00000355710.8:c.2089C>T MANE Select	ENSP00000347942.3:p.Leu697=
NM_001355216.1:c.1327C>T	NP_001342145.1:p.Leu443=
NM_020630.4:c.2089C>T , LRG_518t2:c.2089C>T	NP_065681.1:p.Leu697=
NM_020630.5:c.2089C>T	NP_065681.1:p.Leu697=
NM_020630.6:c.2089C>T	NP_065681.1:p.Leu697=
NM_020975.4:c.2089C>T , LRG_518t1:c.2089C>T	NP_066124.1:p.Leu697=
NM_020975.5:c.2089C>T	NP_066124.1:p.Leu697=
ENST00000340058.5:c.2089C>T	ENSP00000344798.4:p.Leu697=
ENST00000340058.6:c.2089C>T	ENSP00000344798.4:p.Leu697=
ENST00000355710.7:c.2089C>T	ENSP00000347942.3:p.Leu697=
ENST00000615310.4:c.1289+3457C>T	ENSP00000480088.1:n.1289+3457C>T
ENST00000615310.5:c.1693C>T	ENSP00000480088.2:p.Leu565=
ENST00000671844.1:c.*683C>T	ENSP00000500541.1:n.*683C>T
ENST00000672389.1:c.*683C>T	ENSP00000500252.1:n.*683C>T
ENST00000683007.1:n.1663C>T
ENST00000683872.1:n.1654C>T
XM_011540027.1:c.2089C>T	XP_011538329.1:p.Leu697=