Canonical Allele Identifier: CA376770602
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2048904
ClinVar RCV Id: RCV002909429
dbSNP Id: rs1478519389

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100722A>G , CM000672.2:g.43100722A>G GRCh38
NC_000010.10:g.43596170A>G , CM000672.1:g.43596170A>G GRCh37
NC_000010.9:g.42916176A>G NCBI36
NG_007489.1:g.28654A>G , LRG_518:g.28654A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.337A>G ENSP00000480088.2:p.Asn113Asp
ENST00000683278.1:c.239A>G
ENST00000684216.1:c.239A>G
ENST00000340058.6:c.337A>G ENSP00000344798.4:p.Asn113Asp
ENST00000355710.8:c.337A>G MANE Select ENSP00000347942.3:p.Asn113Asp
ENST00000638465.1:c.239A>G
ENST00000640619.1:c.239A>G
ENST00000671844.1:c.337A>G ENSP00000500541.1:p.Asn113Asp
ENST00000672389.1:c.74-10485A>G ENSP00000500252.1:n.74-10485A>G
ENST00000340058.5:c.337A>G ENSP00000344798.4:p.Asn113Asp
ENST00000355710.7:c.337A>G ENSP00000347942.3:p.Asn113Asp
ENST00000498820.5:c.74-11377A>G ENSP00000419080.1:n.74-11377A>G
ENST00000615310.4:c.337A>G ENSP00000480088.1:p.Asn113Asp
NM_020630.4:c.337A>G , LRG_518t2:c.337A>G NP_065681.1:p.Asn113Asp
NM_020975.4:c.337A>G , LRG_518t1:c.337A>G NP_066124.1:p.Asn113Asp
XM_011540027.1:c.337A>G XP_011538329.1:p.Asn113Asp
NM_020630.5:c.337A>G NP_065681.1:p.Asn113Asp
NM_020975.5:c.337A>G NP_066124.1:p.Asn113Asp
NM_020975.6:c.337A>G MANE Select NP_066124.1:p.Asn113Asp
NM_020630.6:c.337A>G NP_065681.1:p.Asn113Asp