Canonical Allele Identifier: CA376543418
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43102542C>G , CM000672.2:g.43102542C>G GRCh38
NC_000010.10:g.43597990C>G , CM000672.1:g.43597990C>G GRCh37
NC_000010.9:g.42917996C>G NCBI36
NG_007489.1:g.30474C>G , LRG_518:g.30474C>G

Transcript Alleles

HGVS Amino-acid Change
NM_020975.6:c.538C>G MANE Select NP_066124.1:p.Arg180Gly
ENST00000355710.8:c.538C>G MANE Select ENSP00000347942.3:p.Arg180Gly
NM_020630.4:c.538C>G , LRG_518t2:c.538C>G NP_065681.1:p.Arg180Gly
NM_020630.5:c.538C>G NP_065681.1:p.Arg180Gly
NM_020630.6:c.538C>G NP_065681.1:p.Arg180Gly
NM_020975.4:c.538C>G , LRG_518t1:c.538C>G NP_066124.1:p.Arg180Gly
NM_020975.5:c.538C>G NP_066124.1:p.Arg180Gly
ENST00000340058.5:c.538C>G ENSP00000344798.4:p.Arg180Gly
ENST00000340058.6:c.538C>G ENSP00000344798.4:p.Arg180Gly
ENST00000355710.7:c.538C>G ENSP00000347942.3:p.Arg180Gly
ENST00000498820.5:c.74-9557C>G ENSP00000419080.1:n.74-9557C>G
ENST00000615310.4:c.538C>G ENSP00000480088.1:p.Arg180Gly
ENST00000615310.5:c.538C>G ENSP00000480088.2:p.Arg180Gly
ENST00000638465.1:c.480C>G
ENST00000640619.1:c.311C>G
ENST00000671844.1:c.538C>G ENSP00000500541.1:p.Arg180Gly
ENST00000672389.1:c.74-8665C>G ENSP00000500252.1:n.74-8665C>G
ENST00000683278.1:c.459C>G
ENST00000684216.1:c.440C>G
XM_011540027.1:c.538C>G XP_011538329.1:p.Arg180Gly