Canonical Allele Identifier: CA008982

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120129C>T , CM000672.2:g.43120129C>T	GRCh38
NC_000010.10:g.43615577C>T , CM000672.1:g.43615577C>T	GRCh37
NC_000010.9:g.42935583C>T	NCBI36
NG_007489.1:g.48061C>T , LRG_518:g.48061C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.2656C>T MANE Select	NP_066124.1:p.Arg886Trp
ENST00000355710.8:c.2656C>T MANE Select	ENSP00000347942.3:p.Arg886Trp
NM_001355216.1:c.1894C>T	NP_001342145.1:p.Arg632Trp
NM_020630.4:c.2656C>T , LRG_518t2:c.2656C>T	NP_065681.1:p.Arg886Trp
NM_020630.5:c.2656C>T	NP_065681.1:p.Arg886Trp
NM_020630.6:c.2656C>T	NP_065681.1:p.Arg886Trp
NM_020975.4:c.2656C>T , LRG_518t1:c.2656C>T	NP_066124.1:p.Arg886Trp
NM_020975.5:c.2656C>T	NP_066124.1:p.Arg886Trp
ENST00000340058.5:c.2656C>T	ENSP00000344798.4:p.Arg886Trp
ENST00000340058.6:c.2656C>T	ENSP00000344798.4:p.Arg886Trp
ENST00000355710.7:c.2656C>T	ENSP00000347942.3:p.Arg886Trp
ENST00000615310.4:c.*5C>T	ENSP00000480088.1:n.*5C>T
ENST00000615310.5:c.2260C>T	ENSP00000480088.2:p.Arg754Trp
ENST00000671844.1:c.*1250C>T	ENSP00000500541.1:n.*1250C>T
ENST00000672389.1:c.*1250C>T	ENSP00000500252.1:n.*1250C>T
ENST00000683007.1:n.2230C>T
ENST00000683872.1:n.2221C>T
XM_011540027.1:c.2656C>T	XP_011538329.1:p.Arg886Trp