Canonical Allele Identifier: CA1905809418
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43106208C= , CM000672.2:g.43106208C= GRCh38
NC_000010.10:g.43601656C= , CM000672.1:g.43601656C= GRCh37
NC_000010.9:g.42921662C= NCBI36
NG_007489.1:g.34140C= , LRG_518:g.34140C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.867+1015C= ENSP00000480088.2:n.867+1015C=
ENST00000683007.1:n.442-168C=
ENST00000340058.6:c.868-168C= ENSP00000344798.4:n.868-168C=
ENST00000355710.8:c.868-168C= MANE Select ENSP00000347942.3:n.868-168C=
ENST00000671844.1:c.625+3579C= ENSP00000500541.1:n.625+3579C=
ENST00000672389.1:c.74-4999C= ENSP00000500252.1:n.74-4999C=
ENST00000340058.5:c.868-168C= ENSP00000344798.4:n.868-168C=
ENST00000355710.7:c.868-168C= ENSP00000347942.3:n.868-168C=
ENST00000479913.1:n.463-168C=
ENST00000498820.5:c.74-5891C= ENSP00000419080.1:n.74-5891C=
ENST00000615310.4:c.868-168C= ENSP00000480088.1:n.868-168C=
NM_020630.4:c.868-168C= , LRG_518t2:c.868-168C= NP_065681.1:n.868-168C=
NM_020975.4:c.868-168C= , LRG_518t1:c.868-168C= NP_066124.1:n.868-168C=
XM_011540027.1:c.868-168C= XP_011538329.1:n.868-168C=
NM_001355216.1:c.106-168C= NP_001342145.1:n.106-168C=
NM_020630.5:c.868-168C= NP_065681.1:n.868-168C=
NM_020975.5:c.868-168C= NP_066124.1:n.868-168C=
NM_020975.6:c.868-168C= MANE Select NP_066124.1:n.868-168C=
NM_020630.6:c.868-168C= NP_065681.1:n.868-168C=