Canonical Allele Identifier: CA1905832984

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130174A= , CM000672.2:g.43130174A=	GRCh38
NC_000010.10:g.43625622A= , CM000672.1:g.43625622A=	GRCh37
NC_000010.9:g.42945628A=	NCBI36
NG_007489.1:g.58106A= , LRG_518:g.58106A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*3420A=	ENSP00000480088.2:n.*3420A=
ENST00000683007.1:n.6213A=
ENST00000355710.8:c.*1905A= MANE Select	ENSP00000347942.3:n.*1905A=
ENST00000355710.7:c.*1905A=	ENSP00000347942.3:n.*1905A=
ENST00000615310.4:c.*2599A=	ENSP00000480088.1:n.*2599A=
NM_020975.4:c.*1905A= , LRG_518t1:c.*1905A=	NP_066124.1:n.*1905A=
XM_011540027.1:c.*673A=	XP_011538329.1:n.*673A=
NM_020975.5:c.*1905A=	NP_066124.1:n.*1905A=
NM_020975.6:c.*1905A= MANE Select	NP_066124.1:n.*1905A=