Canonical Allele Identifier: CA033724

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43111394T>C , CM000672.2:g.43111394T>C	GRCh38
NC_000010.10:g.43606842T>C , CM000672.1:g.43606842T>C	GRCh37
NC_000010.9:g.42926848T>C	NCBI36
NG_007489.1:g.39326T>C , LRG_518:g.39326T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1451T>C MANE Select	NP_066124.1:p.Met484Thr
ENST00000355710.8:c.1451T>C MANE Select	ENSP00000347942.3:p.Met484Thr
NM_001355216.1:c.689T>C	NP_001342145.1:p.Met230Thr
NM_020630.4:c.1451T>C , LRG_518t2:c.1451T>C	NP_065681.1:p.Met484Thr
NM_020630.5:c.1451T>C	NP_065681.1:p.Met484Thr
NM_020630.6:c.1451T>C	NP_065681.1:p.Met484Thr
NM_020975.4:c.1451T>C , LRG_518t1:c.1451T>C	NP_066124.1:p.Met484Thr
NM_020975.5:c.1451T>C	NP_066124.1:p.Met484Thr
ENST00000340058.5:c.1451T>C	ENSP00000344798.4:p.Met484Thr
ENST00000340058.6:c.1451T>C	ENSP00000344798.4:p.Met484Thr
ENST00000355710.7:c.1451T>C	ENSP00000347942.3:p.Met484Thr
ENST00000498820.5:c.74-705T>C	ENSP00000419080.1:n.74-705T>C
ENST00000615310.4:c.1289+162T>C	ENSP00000480088.1:n.1289+162T>C
ENST00000615310.5:c.1055T>C	ENSP00000480088.2:p.Met352Thr
ENST00000671844.1:c.*45T>C	ENSP00000500541.1:n.*45T>C
ENST00000672389.1:c.*45T>C	ENSP00000500252.1:n.*45T>C
ENST00000683007.1:n.1025T>C
ENST00000683872.1:n.212T>C
XM_011540027.1:c.1451T>C	XP_011538329.1:p.Met484Thr