Canonical Allele Identifier: CA1905813456

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114488T= , CM000672.2:g.43114488T=	GRCh38
NC_000010.10:g.43609936T= , CM000672.1:g.43609936T=	GRCh37
NC_000010.9:g.42929942T=	NCBI36
NG_007489.1:g.42420T= , LRG_518:g.42420T=

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1888T= MANE Select	NP_066124.1:p.Cys630=
ENST00000355710.8:c.1888T= MANE Select	ENSP00000347942.3:p.Cys630=
NM_001355216.1:c.1126T=	NP_001342145.1:p.Cys376=
NM_020630.4:c.1888T= , LRG_518t2:c.1888T=	NP_065681.1:p.Cys630=
NM_020630.5:c.1888T=	NP_065681.1:p.Cys630=
NM_020630.6:c.1888T=	NP_065681.1:p.Cys630=
NM_020975.4:c.1888T= , LRG_518t1:c.1888T=	NP_066124.1:p.Cys630=
NM_020975.5:c.1888T=	NP_066124.1:p.Cys630=
ENST00000340058.5:c.1888T=	ENSP00000344798.4:p.Cys630=
ENST00000340058.6:c.1888T=	ENSP00000344798.4:p.Cys630=
ENST00000355710.7:c.1888T=	ENSP00000347942.3:p.Cys630=
ENST00000498820.5:c.439T=	ENSP00000419080.1:p.Cys147=
ENST00000615310.4:c.1289+3256T=	ENSP00000480088.1:n.1289+3256T=
ENST00000615310.5:c.1492T=	ENSP00000480088.2:p.Cys498=
ENST00000671844.1:c.*482T=	ENSP00000500541.1:n.*482T=
ENST00000672389.1:c.*482T=	ENSP00000500252.1:n.*482T=
ENST00000683007.1:n.1462T=
ENST00000683872.1:n.1453T=
XM_011540027.1:c.1888T=	XP_011538329.1:p.Cys630=