Canonical Allele Identifier: CA2787757450

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130195_43130198del , CM000672.2:g.43130195_43130198del	GRCh38
NC_000010.10:g.43625643_43625646del , CM000672.1:g.43625643_43625646del	GRCh37
NC_000010.9:g.42945649_42945652del	NCBI36
NG_007489.1:g.58127_58130del , LRG_518:g.58127_58130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*3441_*3444del	ENSP00000480088.2:n.*3441_*3444del
ENST00000683007.1:n.6234_6237del
ENST00000355710.8:c.*1926_*1929del MANE Select	ENSP00000347942.3:n.*1926_*1929del
ENST00000355710.7:c.*1926_*1929del	ENSP00000347942.3:n.*1926_*1929del
ENST00000615310.4:c.*2620_*2623del	ENSP00000480088.1:n.*2620_*2623del
NM_020975.4:c.*1926_*1929del , LRG_518t1:c.*1926_*1929del	NP_066124.1:n.*1926_*1929del
XM_011540027.1:c.*694_*697del	XP_011538329.1:n.*694_*697del
NM_020975.5:c.*1926_*1929del	NP_066124.1:n.*1926_*1929del
NM_020975.6:c.*1926_*1929del MANE Select	NP_066124.1:n.*1926_*1929del