Canonical Allele Identifier: CA1905813403
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43114393A= , CM000672.2:g.43114393A= GRCh38
NC_000010.10:g.43609841A= , CM000672.1:g.43609841A= GRCh37
NC_000010.9:g.42929847A= NCBI36
NG_007489.1:g.42325A= , LRG_518:g.42325A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1484-87A= ENSP00000480088.2:n.1484-87A=
ENST00000683007.1:n.1454-87A=
ENST00000683872.1:n.1358A=
ENST00000340058.6:c.1880-87A= ENSP00000344798.4:n.1880-87A=
ENST00000355710.8:c.1880-87A= MANE Select ENSP00000347942.3:n.1880-87A=
ENST00000671844.1:c.*474-87A= ENSP00000500541.1:n.*474-87A=
ENST00000672389.1:c.*474-87A= ENSP00000500252.1:n.*474-87A=
ENST00000340058.5:c.1880-87A= ENSP00000344798.4:n.1880-87A=
ENST00000355710.7:c.1880-87A= ENSP00000347942.3:n.1880-87A=
ENST00000498820.5:c.431-87A= ENSP00000419080.1:n.431-87A=
ENST00000615310.4:c.1289+3161A= ENSP00000480088.1:n.1289+3161A=
NM_020630.4:c.1880-87A= , LRG_518t2:c.1880-87A= NP_065681.1:n.1880-87A=
NM_020975.4:c.1880-87A= , LRG_518t1:c.1880-87A= NP_066124.1:n.1880-87A=
XM_011540027.1:c.1880-87A= XP_011538329.1:n.1880-87A=
NM_001355216.1:c.1118-87A= NP_001342145.1:n.1118-87A=
NM_020630.5:c.1880-87A= NP_065681.1:n.1880-87A=
NM_020975.5:c.1880-87A= NP_066124.1:n.1880-87A=
NM_020975.6:c.1880-87A= MANE Select NP_066124.1:n.1880-87A=
NM_020630.6:c.1880-87A= NP_065681.1:n.1880-87A=