Canonical Allele Identifier: CA1905833008

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130213G= , CM000672.2:g.43130213G=	GRCh38
NC_000010.10:g.43625661G= , CM000672.1:g.43625661G=	GRCh37
NC_000010.9:g.42945667G=	NCBI36
NG_007489.1:g.58145G= , LRG_518:g.58145G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*3459G=	ENSP00000480088.2:n.*3459G=
ENST00000683007.1:n.6252G=
ENST00000355710.8:c.*1944G= MANE Select	ENSP00000347942.3:n.*1944G=
ENST00000355710.7:c.*1944G=	ENSP00000347942.3:n.*1944G=
ENST00000615310.4:c.*2638G=	ENSP00000480088.1:n.*2638G=
NM_020975.4:c.*1944G= , LRG_518t1:c.*1944G=	NP_066124.1:n.*1944G=
XM_011540027.1:c.*712G=	XP_011538329.1:n.*712G=
NM_020975.5:c.*1944G=	NP_066124.1:n.*1944G=
NM_020975.6:c.*1944G= MANE Select	NP_066124.1:n.*1944G=