Canonical Allele Identifier: CA1905832993

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130185G= , CM000672.2:g.43130185G=	GRCh38
NC_000010.10:g.43625633G= , CM000672.1:g.43625633G=	GRCh37
NC_000010.9:g.42945639G=	NCBI36
NG_007489.1:g.58117G= , LRG_518:g.58117G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*3431G=	ENSP00000480088.2:n.*3431G=
ENST00000683007.1:n.6224G=
ENST00000355710.8:c.*1916G= MANE Select	ENSP00000347942.3:n.*1916G=
ENST00000355710.7:c.*1916G=	ENSP00000347942.3:n.*1916G=
ENST00000615310.4:c.*2610G=	ENSP00000480088.1:n.*2610G=
NM_020975.4:c.*1916G= , LRG_518t1:c.*1916G=	NP_066124.1:n.*1916G=
XM_011540027.1:c.*684G=	XP_011538329.1:n.*684G=
NM_020975.5:c.*1916G=	NP_066124.1:n.*1916G=
NM_020975.6:c.*1916G= MANE Select	NP_066124.1:n.*1916G=