Canonical Allele Identifier: CA1905833014

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130217_43130220delinsTAAG , CM000672.2:g.43130217_43130220delinsTAAG	GRCh38
NC_000010.10:g.43625665_43625668delinsTAAG , CM000672.1:g.43625665_43625668delinsTAAG	GRCh37
NC_000010.9:g.42945671_42945674delinsTAAG	NCBI36
NG_007489.1:g.58149_58152delinsTAAG , LRG_518:g.58149_58152delinsTAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*3463_*3466delinsTAAG	ENSP00000480088.2:n.*3463_*3466delinsTAAG
ENST00000683007.1:n.6256_6259delinsTAAG
ENST00000355710.8:c.*1948_*1951delinsTAAG MANE Select	ENSP00000347942.3:n.*1948_*1951delinsTAAG
ENST00000355710.7:c.*1948_*1951delinsTAAG	ENSP00000347942.3:n.*1948_*1951delinsTAAG
ENST00000615310.4:c.*2642_*2645delinsTAAG	ENSP00000480088.1:n.*2642_*2645delinsTAAG
NM_020975.4:c.*1948_*1951delinsTAAG , LRG_518t1:c.*1948_*1951delinsTAAG	NP_066124.1:n.*1948_*1951delinsTAAG
XM_011540027.1:c.*716_*719delinsTAAG	XP_011538329.1:n.*716_*719delinsTAAG
NM_020975.5:c.*1948_*1951delinsTAAG	NP_066124.1:n.*1948_*1951delinsTAAG
NM_020975.6:c.*1948_*1951delinsTAAG MANE Select	NP_066124.1:n.*1948_*1951delinsTAAG