Canonical Allele Identifier: CA1905833063

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130297G= , CM000672.2:g.43130297G=	GRCh38
NC_000010.10:g.43625745G= , CM000672.1:g.43625745G=	GRCh37
NC_000010.9:g.42945751G=	NCBI36
NG_007489.1:g.58229G= , LRG_518:g.58229G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355710.8:c.*2028G= MANE Select	ENSP00000347942.3:n.*2028G=
ENST00000355710.7:c.*2028G=	ENSP00000347942.3:n.*2028G=
ENST00000615310.4:c.*2722G=	ENSP00000480088.1:n.*2722G=
NM_020975.4:c.*2028G= , LRG_518t1:c.*2028G=	NP_066124.1:n.*2028G=
XM_011540027.1:c.*796G=	XP_011538329.1:n.*796G=
NM_020975.5:c.*2028G=	NP_066124.1:n.*2028G=
NM_020975.6:c.*2028G= MANE Select	NP_066124.1:n.*2028G=