Canonical Allele Identifier: CA1905826336
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43124892G= , CM000672.2:g.43124892G= GRCh38
NC_000010.10:g.43620340G= , CM000672.1:g.43620340G= GRCh37
NC_000010.9:g.42940346G= NCBI36
NG_007489.1:g.52824G= , LRG_518:g.52824G=

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.2553G= ENSP00000480088.2:p.Leu851=
ENST00000683007.1:n.2523G=
ENST00000340058.6:c.2949G= ENSP00000344798.4:p.Leu983=
ENST00000355710.8:c.2949G= MANE Select ENSP00000347942.3:p.Leu983=
ENST00000671844.1:c.*1543G= ENSP00000500541.1:n.*1543G=
ENST00000672389.1:c.*1543G= ENSP00000500252.1:n.*1543G=
ENST00000340058.5:c.2949G= ENSP00000344798.4:p.Leu983=
ENST00000355710.7:c.2949G= ENSP00000347942.3:p.Leu983=
ENST00000615310.4:c.*298G= ENSP00000480088.1:n.*298G=
NM_020630.4:c.2949G= , LRG_518t2:c.2949G= NP_065681.1:p.Leu983=
NM_020975.4:c.2949G= , LRG_518t1:c.2949G= NP_066124.1:p.Leu983=
XM_011540027.1:c.2949G= XP_011538329.1:p.Leu983=
NM_001355216.1:c.2187G= NP_001342145.1:p.Leu729=
NM_020630.5:c.2949G= NP_065681.1:p.Leu983=
NM_020975.5:c.2949G= NP_066124.1:p.Leu983=
NM_020975.6:c.2949G= MANE Select NP_066124.1:p.Leu983=
NM_020630.6:c.2949G= NP_065681.1:p.Leu983=