Canonical Allele Identifier: CA1905832980
Gene: RET HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130173C= , CM000672.2:g.43130173C= GRCh38
NC_000010.10:g.43625621C= , CM000672.1:g.43625621C= GRCh37
NC_000010.9:g.42945627C= NCBI36
NG_007489.1:g.58105C= , LRG_518:g.58105C=

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3419C= ENSP00000480088.2:n.*3419C=
ENST00000683007.1:n.6212C=
ENST00000355710.8:c.*1904C= MANE Select ENSP00000347942.3:n.*1904C=
ENST00000355710.7:c.*1904C= ENSP00000347942.3:n.*1904C=
ENST00000615310.4:c.*2598C= ENSP00000480088.1:n.*2598C=
NM_020975.4:c.*1904C= , LRG_518t1:c.*1904C= NP_066124.1:n.*1904C=
XM_011540027.1:c.*672C= XP_011538329.1:n.*672C=
NM_020975.5:c.*1904C= NP_066124.1:n.*1904C=
NM_020975.6:c.*1904C= MANE Select NP_066124.1:n.*1904C=
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