Canonical Allele Identifier: CA469027630

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43112149C>A , CM000672.2:g.43112149C>A	GRCh38
NC_000010.10:g.43607597C>A , CM000672.1:g.43607597C>A	GRCh37
NC_000010.9:g.42927603C>A	NCBI36
NG_007489.1:g.40081C>A , LRG_518:g.40081C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1573C>A MANE Select	NP_066124.1:p.Arg525=
ENST00000355710.8:c.1573C>A MANE Select	ENSP00000347942.3:p.Arg525=
NM_001355216.1:c.811C>A	NP_001342145.1:p.Arg271=
NM_020630.4:c.1573C>A , LRG_518t2:c.1573C>A	NP_065681.1:p.Arg525=
NM_020630.5:c.1573C>A	NP_065681.1:p.Arg525=
NM_020630.6:c.1573C>A	NP_065681.1:p.Arg525=
NM_020975.4:c.1573C>A , LRG_518t1:c.1573C>A	NP_066124.1:p.Arg525=
NM_020975.5:c.1573C>A	NP_066124.1:p.Arg525=
ENST00000340058.5:c.1573C>A	ENSP00000344798.4:p.Arg525=
ENST00000340058.6:c.1573C>A	ENSP00000344798.4:p.Arg525=
ENST00000355710.7:c.1573C>A	ENSP00000347942.3:p.Arg525=
ENST00000498820.5:c.124C>A	ENSP00000419080.1:p.Arg42=
ENST00000615310.4:c.1289+917C>A	ENSP00000480088.1:n.1289+917C>A
ENST00000615310.5:c.1177C>A	ENSP00000480088.2:p.Arg393=
ENST00000671844.1:c.*167C>A	ENSP00000500541.1:n.*167C>A
ENST00000672389.1:c.*167C>A	ENSP00000500252.1:n.*167C>A
ENST00000683007.1:n.1147C>A
ENST00000683872.1:n.334C>A
XM_011540027.1:c.1573C>A	XP_011538329.1:p.Arg525=