Canonical Allele Identifier: CA376552765

Gene: RET

Linked Data

• ClinVar Variation Id: 1430721
• ClinVar RCV Id: RCV001952515 ; RCV002407107 ; RCV002503651
• dbSNP Id: rs1837994115
• MyVariant Identifiers: chr10:g.43609073A>G (hg19) ; chr10:g.43113625A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113625A>G , CM000672.2:g.43113625A>G	GRCh38
NC_000010.10:g.43609073A>G , CM000672.1:g.43609073A>G	GRCh37
NC_000010.9:g.42929079A>G	NCBI36
NG_007489.1:g.41557A>G , LRG_518:g.41557A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1433A>G	ENSP00000480088.2:p.Asn478Ser
ENST00000683007.1:n.1403A>G
ENST00000683872.1:n.590A>G
ENST00000340058.6:c.1829A>G	ENSP00000344798.4:p.Asn610Ser
ENST00000355710.8:c.1829A>G MANE Select	ENSP00000347942.3:p.Asn610Ser
ENST00000671844.1:c.*423A>G	ENSP00000500541.1:n.*423A>G
ENST00000672389.1:c.*423A>G	ENSP00000500252.1:n.*423A>G
ENST00000340058.5:c.1829A>G	ENSP00000344798.4:p.Asn610Ser
ENST00000355710.7:c.1829A>G	ENSP00000347942.3:p.Asn610Ser
ENST00000498820.5:c.380A>G	ENSP00000419080.1:p.Asn127Ser
ENST00000615310.4:c.1289+2393A>G	ENSP00000480088.1:n.1289+2393A>G
NM_020630.4:c.1829A>G , LRG_518t2:c.1829A>G	NP_065681.1:p.Asn610Ser
NM_020975.4:c.1829A>G , LRG_518t1:c.1829A>G	NP_066124.1:p.Asn610Ser
XM_011540027.1:c.1829A>G	XP_011538329.1:p.Asn610Ser
NM_001355216.1:c.1067A>G	NP_001342145.1:p.Asn356Ser
NM_020630.5:c.1829A>G	NP_065681.1:p.Asn610Ser
NM_020975.5:c.1829A>G	NP_066124.1:p.Asn610Ser
NM_020975.6:c.1829A>G MANE Select	NP_066124.1:p.Asn610Ser
NM_020630.6:c.1829A>G	NP_065681.1:p.Asn610Ser