Canonical Allele Identifier: CA1905826312

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43124887C= , CM000672.2:g.43124887C=	GRCh38
NC_000010.10:g.43620335C= , CM000672.1:g.43620335C=	GRCh37
NC_000010.9:g.42940341C=	NCBI36
NG_007489.1:g.52819C= , LRG_518:g.52819C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.2944C= MANE Select	NP_066124.1:p.Arg982=
ENST00000355710.8:c.2944C= MANE Select	ENSP00000347942.3:p.Arg982=
NM_001355216.1:c.2182C=	NP_001342145.1:p.Arg728=
NM_020630.4:c.2944C= , LRG_518t2:c.2944C=	NP_065681.1:p.Arg982=
NM_020630.5:c.2944C=	NP_065681.1:p.Arg982=
NM_020630.6:c.2944C=	NP_065681.1:p.Arg982=
NM_020975.4:c.2944C= , LRG_518t1:c.2944C=	NP_066124.1:p.Arg982=
NM_020975.5:c.2944C=	NP_066124.1:p.Arg982=
ENST00000340058.5:c.2944C=	ENSP00000344798.4:p.Arg982=
ENST00000340058.6:c.2944C=	ENSP00000344798.4:p.Arg982=
ENST00000355710.7:c.2944C=	ENSP00000347942.3:p.Arg982=
ENST00000615310.4:c.*293C=	ENSP00000480088.1:n.*293C=
ENST00000615310.5:c.2548C=	ENSP00000480088.2:p.Arg850=
ENST00000671844.1:c.*1538C=	ENSP00000500541.1:n.*1538C=
ENST00000672389.1:c.*1538C=	ENSP00000500252.1:n.*1538C=
ENST00000683007.1:n.2518C=
XM_011540027.1:c.2944C=	XP_011538329.1:p.Arg982=