Canonical Allele Identifier: CA040485
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1558816
dbSNP Id: rs1800863

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43120185C>A , CM000672.2:g.43120185C>A GRCh38
NC_000010.10:g.43615633C>A , CM000672.1:g.43615633C>A GRCh37
NC_000010.9:g.42935639C>A NCBI36
NG_007489.1:g.48117C>A , LRG_518:g.48117C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.2316C>A ENSP00000480088.2:p.Ser772=
ENST00000683007.1:n.2286C>A
ENST00000683872.1:n.2277C>A
ENST00000340058.6:c.2712C>A ENSP00000344798.4:p.Ser904=
ENST00000355710.8:c.2712C>A MANE Select ENSP00000347942.3:p.Ser904=
ENST00000671844.1:c.*1306C>A ENSP00000500541.1:n.*1306C>A
ENST00000672389.1:c.*1306C>A ENSP00000500252.1:n.*1306C>A
ENST00000340058.5:c.2712C>A ENSP00000344798.4:p.Ser904=
ENST00000355710.7:c.2712C>A ENSP00000347942.3:p.Ser904=
ENST00000615310.4:c.*61C>A ENSP00000480088.1:n.*61C>A
NM_020630.4:c.2712C>A , LRG_518t2:c.2712C>A NP_065681.1:p.Ser904=
NM_020975.4:c.2712C>A , LRG_518t1:c.2712C>A NP_066124.1:p.Ser904=
XM_011540027.1:c.2712C>A XP_011538329.1:p.Ser904=
NM_001355216.1:c.1950C>A NP_001342145.1:p.Ser650=
NM_020630.5:c.2712C>A NP_065681.1:p.Ser904=
NM_020975.5:c.2712C>A NP_066124.1:p.Ser904=
NM_020975.6:c.2712C>A MANE Select NP_066124.1:p.Ser904=
NM_020630.6:c.2712C>A NP_065681.1:p.Ser904=