Canonical Allele Identifier: CA1905813018
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43113546C= , CM000672.2:g.43113546C= GRCh38
NC_000010.10:g.43608994C= , CM000672.1:g.43608994C= GRCh37
NC_000010.9:g.42929000C= NCBI36
NG_007489.1:g.41478C= , LRG_518:g.41478C=

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1364-10C= ENSP00000480088.2:n.1364-10C=
ENST00000683007.1:n.1334-10C=
ENST00000683872.1:n.521-10C=
ENST00000340058.6:c.1760-10C= ENSP00000344798.4:n.1760-10C=
ENST00000355710.8:c.1760-10C= MANE Select ENSP00000347942.3:n.1760-10C=
ENST00000671844.1:c.*354-10C= ENSP00000500541.1:n.*354-10C=
ENST00000672389.1:c.*354-10C= ENSP00000500252.1:n.*354-10C=
ENST00000340058.5:c.1760-10C= ENSP00000344798.4:n.1760-10C=
ENST00000355710.7:c.1760-10C= ENSP00000347942.3:n.1760-10C=
ENST00000498820.5:c.311-10C= ENSP00000419080.1:n.311-10C=
ENST00000615310.4:c.1289+2314C= ENSP00000480088.1:n.1289+2314C=
NM_020630.4:c.1760-10C= , LRG_518t2:c.1760-10C= NP_065681.1:n.1760-10C=
NM_020975.4:c.1760-10C= , LRG_518t1:c.1760-10C= NP_066124.1:n.1760-10C=
XM_011540027.1:c.1760-10C= XP_011538329.1:n.1760-10C=
NM_001355216.1:c.998-10C= NP_001342145.1:n.998-10C=
NM_020630.5:c.1760-10C= NP_065681.1:n.1760-10C=
NM_020975.5:c.1760-10C= NP_066124.1:n.1760-10C=
NM_020975.6:c.1760-10C= MANE Select NP_066124.1:n.1760-10C=
NM_020630.6:c.1760-10C= NP_065681.1:n.1760-10C=