Canonical Allele Identifier: CA1905825065

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43123783A= , CM000672.2:g.43123783A=	GRCh38
NC_000010.10:g.43619231A= , CM000672.1:g.43619231A=	GRCh37
NC_000010.9:g.42939237A=	NCBI36
NG_007489.1:g.51715A= , LRG_518:g.51715A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2518A=	ENSP00000480088.2:p.Arg840=
ENST00000683007.1:n.2488A=
ENST00000340058.6:c.2914A=	ENSP00000344798.4:p.Arg972=
ENST00000355710.8:c.2914A= MANE Select	ENSP00000347942.3:p.Arg972=
ENST00000671844.1:c.*1508A=	ENSP00000500541.1:n.*1508A=
ENST00000672389.1:c.*1508A=	ENSP00000500252.1:n.*1508A=
ENST00000340058.5:c.2914A=	ENSP00000344798.4:p.Arg972=
ENST00000355710.7:c.2914A=	ENSP00000347942.3:p.Arg972=
ENST00000615310.4:c.*263A=	ENSP00000480088.1:n.*263A=
NM_020630.4:c.2914A= , LRG_518t2:c.2914A=	NP_065681.1:p.Arg972=
NM_020975.4:c.2914A= , LRG_518t1:c.2914A=	NP_066124.1:p.Arg972=
XM_011540027.1:c.2914A=	XP_011538329.1:p.Arg972=
NM_001355216.1:c.2152A=	NP_001342145.1:p.Arg718=
NM_020630.5:c.2914A=	NP_065681.1:p.Arg972=
NM_020975.5:c.2914A=	NP_066124.1:p.Arg972=
NM_020975.6:c.2914A= MANE Select	NP_066124.1:p.Arg972=
NM_020630.6:c.2914A=	NP_065681.1:p.Arg972=