Canonical Allele Identifier: CA008672
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24937
dbSNP Id: rs377767415

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43118418A>G , CM000672.2:g.43118418A>G GRCh38
NC_000010.10:g.43613866A>G , CM000672.1:g.43613866A>G GRCh37
NC_000010.9:g.42933872A>G NCBI36
NG_007489.1:g.46350A>G , LRG_518:g.46350A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1934A>G ENSP00000480088.2:p.Asn645Ser
ENST00000683007.1:n.1904A>G
ENST00000683872.1:n.1895A>G
ENST00000340058.6:c.2330A>G ENSP00000344798.4:p.Asn777Ser
ENST00000355710.8:c.2330A>G MANE Select ENSP00000347942.3:p.Asn777Ser
ENST00000671844.1:c.*924A>G ENSP00000500541.1:n.*924A>G
ENST00000672389.1:c.*924A>G ENSP00000500252.1:n.*924A>G
ENST00000340058.5:c.2330A>G ENSP00000344798.4:p.Asn777Ser
ENST00000355710.7:c.2330A>G ENSP00000347942.3:p.Asn777Ser
ENST00000615310.4:c.1290-1284A>G ENSP00000480088.1:n.1290-1284A>G
NM_020630.4:c.2330A>G , LRG_518t2:c.2330A>G NP_065681.1:p.Asn777Ser
NM_020975.4:c.2330A>G , LRG_518t1:c.2330A>G NP_066124.1:p.Asn777Ser
XM_011540027.1:c.2330A>G XP_011538329.1:p.Asn777Ser
NM_001355216.1:c.1568A>G NP_001342145.1:p.Asn523Ser
NM_020630.5:c.2330A>G NP_065681.1:p.Asn777Ser
NM_020975.5:c.2330A>G NP_066124.1:p.Asn777Ser
NM_020975.6:c.2330A>G MANE Select NP_066124.1:p.Asn777Ser
NM_020630.6:c.2330A>G NP_065681.1:p.Asn777Ser