Canonical Allele Identifier: CA1905814007

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077077G= , CM000672.2:g.43077077G=	GRCh38
NC_000010.10:g.43572525G= , CM000672.1:g.43572525G=	GRCh37
NC_000010.9:g.42892531G=	NCBI36
NG_007489.1:g.5009G= , LRG_518:g.5009G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340058.6:c.-182G=	ENSP00000344798.4:n.-182G=
ENST00000355710.8:c.-182G= MANE Select	ENSP00000347942.3:n.-182G=
ENST00000671844.1:c.-182G=	ENSP00000500541.1:n.-182G=
ENST00000672389.1:c.-182G=	ENSP00000500252.1:n.-182G=
ENST00000355710.7:c.-182G=	ENSP00000347942.3:n.-182G=
ENST00000498820.5:c.-182G=	ENSP00000419080.1:n.-182G=
ENST00000615310.4:c.-182G=	ENSP00000480088.1:n.-182G=
NM_020630.4:c.-182G= , LRG_518t2:c.-182G=	NP_065681.1:n.-182G=
NM_020975.4:c.-182G= , LRG_518t1:c.-182G=	NP_066124.1:n.-182G=
XM_011540027.1:c.-182G=	XP_011538329.1:n.-182G=
NM_020630.5:c.-182G=	NP_065681.1:n.-182G=
NM_020975.5:c.-182G=	NP_066124.1:n.-182G=
NM_020975.6:c.-182G= MANE Select	NP_066124.1:n.-182G=
NM_020630.6:c.-182G=	NP_065681.1:n.-182G=