Canonical Allele Identifier: CA2608897194
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43130303-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130303A>G , CM000672.2:g.43130303A>G GRCh38
NC_000010.10:g.43625751A>G , CM000672.1:g.43625751A>G GRCh37
NC_000010.9:g.42945757A>G NCBI36
NG_007489.1:g.58235A>G , LRG_518:g.58235A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2034A>G MANE Select ENSP00000347942.3:n.*2034A>G
ENST00000355710.7:c.*2034A>G ENSP00000347942.3:n.*2034A>G
ENST00000615310.4:c.*2728A>G ENSP00000480088.1:n.*2728A>G
NM_020975.4:c.*2034A>G , LRG_518t1:c.*2034A>G NP_066124.1:n.*2034A>G
XM_011540027.1:c.*802A>G XP_011538329.1:n.*802A>G
NM_020975.5:c.*2034A>G NP_066124.1:n.*2034A>G
NM_020975.6:c.*2034A>G MANE Select NP_066124.1:n.*2034A>G
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