Canonical Allele Identifier: CA1905817799

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118487C= , CM000672.2:g.43118487C=	GRCh38
NC_000010.10:g.43613935C= , CM000672.1:g.43613935C=	GRCh37
NC_000010.9:g.42933941C=	NCBI36
NG_007489.1:g.46419C= , LRG_518:g.46419C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1996+7C=	ENSP00000480088.2:n.1996+7C=
ENST00000683007.1:n.1966+7C=
ENST00000683872.1:n.1957+7C=
ENST00000340058.6:c.2392+7C=	ENSP00000344798.4:n.2392+7C=
ENST00000355710.8:c.2392+7C= MANE Select	ENSP00000347942.3:n.2392+7C=
ENST00000671844.1:c.*986+7C=	ENSP00000500541.1:n.*986+7C=
ENST00000672389.1:c.*986+7C=	ENSP00000500252.1:n.*986+7C=
ENST00000340058.5:c.2392+7C=	ENSP00000344798.4:n.2392+7C=
ENST00000355710.7:c.2392+7C=	ENSP00000347942.3:n.2392+7C=
ENST00000615310.4:c.1290-1215C=	ENSP00000480088.1:n.1290-1215C=
NM_020630.4:c.2392+7C= , LRG_518t2:c.2392+7C=	NP_065681.1:n.2392+7C=
NM_020975.4:c.2392+7C= , LRG_518t1:c.2392+7C=	NP_066124.1:n.2392+7C=
XM_011540027.1:c.2392+7C=	XP_011538329.1:n.2392+7C=
NM_001355216.1:c.1630+7C=	NP_001342145.1:n.1630+7C=
NM_020630.5:c.2392+7C=	NP_065681.1:n.2392+7C=
NM_020975.5:c.2392+7C=	NP_066124.1:n.2392+7C=
NM_020975.6:c.2392+7C= MANE Select	NP_066124.1:n.2392+7C=
NM_020630.6:c.2392+7C=	NP_065681.1:n.2392+7C=