Canonical Allele Identifier: CA1905813527

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114596A= , CM000672.2:g.43114596A=	GRCh38
NC_000010.10:g.43610044A= , CM000672.1:g.43610044A=	GRCh37
NC_000010.9:g.42930050A=	NCBI36
NG_007489.1:g.42528A= , LRG_518:g.42528A=

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1996A= MANE Select	NP_066124.1:p.Lys666=
ENST00000355710.8:c.1996A= MANE Select	ENSP00000347942.3:p.Lys666=
NM_001355216.1:c.1234A=	NP_001342145.1:p.Lys412=
NM_020630.4:c.1996A= , LRG_518t2:c.1996A=	NP_065681.1:p.Lys666=
NM_020630.5:c.1996A=	NP_065681.1:p.Lys666=
NM_020630.6:c.1996A=	NP_065681.1:p.Lys666=
NM_020975.4:c.1996A= , LRG_518t1:c.1996A=	NP_066124.1:p.Lys666=
NM_020975.5:c.1996A=	NP_066124.1:p.Lys666=
ENST00000340058.5:c.1996A=	ENSP00000344798.4:p.Lys666=
ENST00000340058.6:c.1996A=	ENSP00000344798.4:p.Lys666=
ENST00000355710.7:c.1996A=	ENSP00000347942.3:p.Lys666=
ENST00000615310.4:c.1289+3364A=	ENSP00000480088.1:n.1289+3364A=
ENST00000615310.5:c.1600A=	ENSP00000480088.2:p.Lys534=
ENST00000671844.1:c.*590A=	ENSP00000500541.1:n.*590A=
ENST00000672389.1:c.*590A=	ENSP00000500252.1:n.*590A=
ENST00000683007.1:n.1570A=
ENST00000683872.1:n.1561A=
XM_011540027.1:c.1996A=	XP_011538329.1:p.Lys666=