Canonical Allele Identifier: CA1905814011

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077081G= , CM000672.2:g.43077081G=	GRCh38
NC_000010.10:g.43572529G= , CM000672.1:g.43572529G=	GRCh37
NC_000010.9:g.42892535G=	NCBI36
NG_007489.1:g.5013G= , LRG_518:g.5013G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000340058.6:c.-178G=	ENSP00000344798.4:n.-178G=
ENST00000355710.8:c.-178G= MANE Select	ENSP00000347942.3:n.-178G=
ENST00000671844.1:c.-178G=	ENSP00000500541.1:n.-178G=
ENST00000672389.1:c.-178G=	ENSP00000500252.1:n.-178G=
ENST00000340058.5:c.-178G=	ENSP00000344798.4:n.-178G=
ENST00000355710.7:c.-178G=	ENSP00000347942.3:n.-178G=
ENST00000498820.5:c.-178G=	ENSP00000419080.1:n.-178G=
ENST00000615310.4:c.-178G=	ENSP00000480088.1:n.-178G=
NM_020630.4:c.-178G= , LRG_518t2:c.-178G=	NP_065681.1:n.-178G=
NM_020975.4:c.-178G= , LRG_518t1:c.-178G=	NP_066124.1:n.-178G=
XM_011540027.1:c.-178G=	XP_011538329.1:n.-178G=
NM_020630.5:c.-178G=	NP_065681.1:n.-178G=
NM_020975.5:c.-178G=	NP_066124.1:n.-178G=
NM_020975.6:c.-178G= MANE Select	NP_066124.1:n.-178G=
NM_020630.6:c.-178G=	NP_065681.1:n.-178G=