Canonical Allele Identifier: CA206261749

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43112142C>T , CM000672.2:g.43112142C>T	GRCh38
NC_000010.10:g.43607590C>T , CM000672.1:g.43607590C>T	GRCh37
NC_000010.9:g.42927596C>T	NCBI36
NG_007489.1:g.40074C>T , LRG_518:g.40074C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1566C>T MANE Select	NP_066124.1:p.Ser522=
ENST00000355710.8:c.1566C>T MANE Select	ENSP00000347942.3:p.Ser522=
NM_001355216.1:c.804C>T	NP_001342145.1:p.Ser268=
NM_020630.4:c.1566C>T , LRG_518t2:c.1566C>T	NP_065681.1:p.Ser522=
NM_020630.5:c.1566C>T	NP_065681.1:p.Ser522=
NM_020630.6:c.1566C>T	NP_065681.1:p.Ser522=
NM_020975.4:c.1566C>T , LRG_518t1:c.1566C>T	NP_066124.1:p.Ser522=
NM_020975.5:c.1566C>T	NP_066124.1:p.Ser522=
ENST00000340058.5:c.1566C>T	ENSP00000344798.4:p.Ser522=
ENST00000340058.6:c.1566C>T	ENSP00000344798.4:p.Ser522=
ENST00000355710.7:c.1566C>T	ENSP00000347942.3:p.Ser522=
ENST00000498820.5:c.117C>T	ENSP00000419080.1:p.Ser39=
ENST00000615310.4:c.1289+910C>T	ENSP00000480088.1:n.1289+910C>T
ENST00000615310.5:c.1170C>T	ENSP00000480088.2:p.Ser390=
ENST00000671844.1:c.*160C>T	ENSP00000500541.1:n.*160C>T
ENST00000672389.1:c.*160C>T	ENSP00000500252.1:n.*160C>T
ENST00000683007.1:n.1140C>T
ENST00000683872.1:n.327C>T
XM_011540027.1:c.1566C>T	XP_011538329.1:p.Ser522=