Canonical Allele Identifier: CA1905833016

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130219A= , CM000672.2:g.43130219A=	GRCh38
NC_000010.10:g.43625667A= , CM000672.1:g.43625667A=	GRCh37
NC_000010.9:g.42945673A=	NCBI36
NG_007489.1:g.58151A= , LRG_518:g.58151A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*3465A=	ENSP00000480088.2:n.*3465A=
ENST00000683007.1:n.6258A=
ENST00000355710.8:c.*1950A= MANE Select	ENSP00000347942.3:n.*1950A=
ENST00000355710.7:c.*1950A=	ENSP00000347942.3:n.*1950A=
ENST00000615310.4:c.*2644A=	ENSP00000480088.1:n.*2644A=
NM_020975.4:c.*1950A= , LRG_518t1:c.*1950A=	NP_066124.1:n.*1950A=
XM_011540027.1:c.*718A=	XP_011538329.1:n.*718A=
NM_020975.5:c.*1950A=	NP_066124.1:n.*1950A=
NM_020975.6:c.*1950A= MANE Select	NP_066124.1:n.*1950A=