Canonical Allele Identifier: CA1905817732

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118454A= , CM000672.2:g.43118454A=	GRCh38
NC_000010.10:g.43613902A= , CM000672.1:g.43613902A=	GRCh37
NC_000010.9:g.42933908A=	NCBI36
NG_007489.1:g.46386A= , LRG_518:g.46386A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1970A=	ENSP00000480088.2:p.Lys657=
ENST00000683007.1:n.1940A=
ENST00000683872.1:n.1931A=
ENST00000340058.6:c.2366A=	ENSP00000344798.4:p.Lys789=
ENST00000355710.8:c.2366A= MANE Select	ENSP00000347942.3:p.Lys789=
ENST00000671844.1:c.*960A=	ENSP00000500541.1:n.*960A=
ENST00000672389.1:c.*960A=	ENSP00000500252.1:n.*960A=
ENST00000340058.5:c.2366A=	ENSP00000344798.4:p.Lys789=
ENST00000355710.7:c.2366A=	ENSP00000347942.3:p.Lys789=
ENST00000615310.4:c.1290-1248A=	ENSP00000480088.1:n.1290-1248A=
NM_020630.4:c.2366A= , LRG_518t2:c.2366A=	NP_065681.1:p.Lys789=
NM_020975.4:c.2366A= , LRG_518t1:c.2366A=	NP_066124.1:p.Lys789=
XM_011540027.1:c.2366A=	XP_011538329.1:p.Lys789=
NM_001355216.1:c.1604A=	NP_001342145.1:p.Lys535=
NM_020630.5:c.2366A=	NP_065681.1:p.Lys789=
NM_020975.5:c.2366A=	NP_066124.1:p.Lys789=
NM_020975.6:c.2366A= MANE Select	NP_066124.1:p.Lys789=
NM_020630.6:c.2366A=	NP_065681.1:p.Lys789=