Canonical Allele Identifier: CA1905822176

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43121950G= , CM000672.2:g.43121950G=	GRCh38
NC_000010.10:g.43617398G= , CM000672.1:g.43617398G=	GRCh37
NC_000010.9:g.42937404G=	NCBI36
NG_007489.1:g.49882G= , LRG_518:g.49882G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.2735G= MANE Select	NP_066124.1:p.Arg912=
ENST00000355710.8:c.2735G= MANE Select	ENSP00000347942.3:p.Arg912=
NM_001355216.1:c.1973G=	NP_001342145.1:p.Arg658=
NM_020630.4:c.2735G= , LRG_518t2:c.2735G=	NP_065681.1:p.Arg912=
NM_020630.5:c.2735G=	NP_065681.1:p.Arg912=
NM_020630.6:c.2735G=	NP_065681.1:p.Arg912=
NM_020975.4:c.2735G= , LRG_518t1:c.2735G=	NP_066124.1:p.Arg912=
NM_020975.5:c.2735G=	NP_066124.1:p.Arg912=
ENST00000340058.5:c.2735G=	ENSP00000344798.4:p.Arg912=
ENST00000340058.6:c.2735G=	ENSP00000344798.4:p.Arg912=
ENST00000355710.7:c.2735G=	ENSP00000347942.3:p.Arg912=
ENST00000615310.4:c.*84G=	ENSP00000480088.1:n.*84G=
ENST00000615310.5:c.2339G=	ENSP00000480088.2:p.Arg780=
ENST00000671844.1:c.*1329G=	ENSP00000500541.1:n.*1329G=
ENST00000672389.1:c.*1329G=	ENSP00000500252.1:n.*1329G=
ENST00000683007.1:n.2309G=
XM_011540027.1:c.2735G=	XP_011538329.1:p.Arg912=