Canonical Allele Identifier: CA1905833013

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130217T= , CM000672.2:g.43130217T=	GRCh38
NC_000010.10:g.43625665T= , CM000672.1:g.43625665T=	GRCh37
NC_000010.9:g.42945671T=	NCBI36
NG_007489.1:g.58149T= , LRG_518:g.58149T=

Transcript Alleles

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