Canonical Allele Identifier: CA1905819943

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120158G= , CM000672.2:g.43120158G=	GRCh38
NC_000010.10:g.43615606G= , CM000672.1:g.43615606G=	GRCh37
NC_000010.9:g.42935612G=	NCBI36
NG_007489.1:g.48090G= , LRG_518:g.48090G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2289G=	ENSP00000480088.2:p.Leu763=
ENST00000683007.1:n.2259G=
ENST00000683872.1:n.2250G=
ENST00000340058.6:c.2685G=	ENSP00000344798.4:p.Leu895=
ENST00000355710.8:c.2685G= MANE Select	ENSP00000347942.3:p.Leu895=
ENST00000671844.1:c.*1279G=	ENSP00000500541.1:n.*1279G=
ENST00000672389.1:c.*1279G=	ENSP00000500252.1:n.*1279G=
ENST00000340058.5:c.2685G=	ENSP00000344798.4:p.Leu895=
ENST00000355710.7:c.2685G=	ENSP00000347942.3:p.Leu895=
ENST00000615310.4:c.*34G=	ENSP00000480088.1:n.*34G=
NM_020630.4:c.2685G= , LRG_518t2:c.2685G=	NP_065681.1:p.Leu895=
NM_020975.4:c.2685G= , LRG_518t1:c.2685G=	NP_066124.1:p.Leu895=
XM_011540027.1:c.2685G=	XP_011538329.1:p.Leu895=
NM_001355216.1:c.1923G=	NP_001342145.1:p.Leu641=
NM_020630.5:c.2685G=	NP_065681.1:p.Leu895=
NM_020975.5:c.2685G=	NP_066124.1:p.Leu895=
NM_020975.6:c.2685G= MANE Select	NP_066124.1:p.Leu895=
NM_020630.6:c.2685G=	NP_065681.1:p.Leu895=