Canonical Allele Identifier: CA1905836847
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100665C= , CM000672.2:g.43100665C= GRCh38
NC_000010.10:g.43596113C= , CM000672.1:g.43596113C= GRCh37
NC_000010.9:g.42916119C= NCBI36
NG_007489.1:g.28597C= , LRG_518:g.28597C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.280C= ENSP00000480088.2:p.Leu94=
ENST00000683278.1:c.182C=
ENST00000684216.1:c.182C=
ENST00000340058.6:c.280C= ENSP00000344798.4:p.Leu94=
ENST00000355710.8:c.280C= MANE Select ENSP00000347942.3:p.Leu94=
ENST00000638465.1:c.182C=
ENST00000640619.1:c.182C=
ENST00000671844.1:c.280C= ENSP00000500541.1:p.Leu94=
ENST00000672389.1:c.74-10542C= ENSP00000500252.1:n.74-10542C=
ENST00000340058.5:c.280C= ENSP00000344798.4:p.Leu94=
ENST00000355710.7:c.280C= ENSP00000347942.3:p.Leu94=
ENST00000498820.5:c.74-11434C= ENSP00000419080.1:n.74-11434C=
ENST00000615310.4:c.280C= ENSP00000480088.1:p.Leu94=
NM_020630.4:c.280C= , LRG_518t2:c.280C= NP_065681.1:p.Leu94=
NM_020975.4:c.280C= , LRG_518t1:c.280C= NP_066124.1:p.Leu94=
XM_011540027.1:c.280C= XP_011538329.1:p.Leu94=
NM_020630.5:c.280C= NP_065681.1:p.Leu94=
NM_020975.5:c.280C= NP_066124.1:p.Leu94=
NM_020975.6:c.280C= MANE Select NP_066124.1:p.Leu94=
NM_020630.6:c.280C= NP_065681.1:p.Leu94=