Canonical Allele Identifier: CA1905814116

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077216C= , CM000672.2:g.43077216C=	GRCh38
NC_000010.10:g.43572664C= , CM000672.1:g.43572664C=	GRCh37
NC_000010.9:g.42892670C=	NCBI36
NG_007489.1:g.5148C= , LRG_518:g.5148C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.-43C=	ENSP00000480088.2:n.-43C=
ENST00000340058.6:c.-43C=	ENSP00000344798.4:n.-43C=
ENST00000355710.8:c.-43C= MANE Select	ENSP00000347942.3:n.-43C=
ENST00000671844.1:c.-43C=	ENSP00000500541.1:n.-43C=
ENST00000672389.1:c.-43C=	ENSP00000500252.1:n.-43C=
ENST00000340058.5:c.-43C=	ENSP00000344798.4:n.-43C=
ENST00000355710.7:c.-43C=	ENSP00000347942.3:n.-43C=
ENST00000498820.5:c.-43C=	ENSP00000419080.1:n.-43C=
ENST00000615310.4:c.-43C=	ENSP00000480088.1:n.-43C=
NM_020630.4:c.-43C= , LRG_518t2:c.-43C=	NP_065681.1:n.-43C=
NM_020975.4:c.-43C= , LRG_518t1:c.-43C=	NP_066124.1:n.-43C=
XM_011540027.1:c.-43C=	XP_011538329.1:n.-43C=
NM_020630.5:c.-43C=	NP_065681.1:n.-43C=
NM_020975.5:c.-43C=	NP_066124.1:n.-43C=
NM_020975.6:c.-43C= MANE Select	NP_066124.1:n.-43C=
NM_020630.6:c.-43C=	NP_065681.1:n.-43C=