Canonical Allele Identifier: CA1905813518

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114583C= , CM000672.2:g.43114583C=	GRCh38
NC_000010.10:g.43610031C= , CM000672.1:g.43610031C=	GRCh37
NC_000010.9:g.42930037C=	NCBI36
NG_007489.1:g.42515C= , LRG_518:g.42515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1587C=	ENSP00000480088.2:p.His529=
ENST00000683007.1:n.1557C=
ENST00000683872.1:n.1548C=
ENST00000340058.6:c.1983C=	ENSP00000344798.4:p.His661=
ENST00000355710.8:c.1983C= MANE Select	ENSP00000347942.3:p.His661=
ENST00000671844.1:c.*577C=	ENSP00000500541.1:n.*577C=
ENST00000672389.1:c.*577C=	ENSP00000500252.1:n.*577C=
ENST00000340058.5:c.1983C=	ENSP00000344798.4:p.His661=
ENST00000355710.7:c.1983C=	ENSP00000347942.3:p.His661=
ENST00000498820.5:c.534C=	ENSP00000419080.1:p.His178=
ENST00000615310.4:c.1289+3351C=	ENSP00000480088.1:n.1289+3351C=
NM_020630.4:c.1983C= , LRG_518t2:c.1983C=	NP_065681.1:p.His661=
NM_020975.4:c.1983C= , LRG_518t1:c.1983C=	NP_066124.1:p.His661=
XM_011540027.1:c.1983C=	XP_011538329.1:p.His661=
NM_001355216.1:c.1221C=	NP_001342145.1:p.His407=
NM_020630.5:c.1983C=	NP_065681.1:p.His661=
NM_020975.5:c.1983C=	NP_066124.1:p.His661=
NM_020975.6:c.1983C= MANE Select	NP_066124.1:p.His661=
NM_020630.6:c.1983C=	NP_065681.1:p.His661=