Canonical Allele Identifier: CA376557053

Gene: RET

Linked Data

• ClinVar Variation Id: 1794014
• ClinVar RCV Id: RCV002437252 ; RCV003533262
• dbSNP Id: rs1322978575
• gnomAD v2: 10-43615549-A-G
• gnomAD v4: 10-43120101-A-G
• MyVariant Identifiers: chr10:g.43615549A>G (hg19) ; chr10:g.43120101A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120101A>G , CM000672.2:g.43120101A>G	GRCh38
NC_000010.10:g.43615549A>G , CM000672.1:g.43615549A>G	GRCh37
NC_000010.9:g.42935555A>G	NCBI36
NG_007489.1:g.48033A>G , LRG_518:g.48033A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2232A>G	ENSP00000480088.2:p.Ala744=
ENST00000683007.1:n.2202A>G
ENST00000683872.1:n.2193A>G
ENST00000340058.6:c.2628A>G	ENSP00000344798.4:p.Ala876=
ENST00000355710.8:c.2628A>G MANE Select	ENSP00000347942.3:p.Ala876=
ENST00000671844.1:c.*1222A>G	ENSP00000500541.1:n.*1222A>G
ENST00000672389.1:c.*1222A>G	ENSP00000500252.1:n.*1222A>G
ENST00000340058.5:c.2628A>G	ENSP00000344798.4:p.Ala876=
ENST00000355710.7:c.2628A>G	ENSP00000347942.3:p.Ala876=
ENST00000615310.4:c.1354A>G	ENSP00000480088.1:p.Ser452Gly
NM_020630.4:c.2628A>G , LRG_518t2:c.2628A>G	NP_065681.1:p.Ala876=
NM_020975.4:c.2628A>G , LRG_518t1:c.2628A>G	NP_066124.1:p.Ala876=
XM_011540027.1:c.2628A>G	XP_011538329.1:p.Ala876=
NM_001355216.1:c.1866A>G	NP_001342145.1:p.Ala622=
NM_020630.5:c.2628A>G	NP_065681.1:p.Ala876=
NM_020975.5:c.2628A>G	NP_066124.1:p.Ala876=
NM_020975.6:c.2628A>G MANE Select	NP_066124.1:p.Ala876=
NM_020630.6:c.2628A>G	NP_065681.1:p.Ala876=