Canonical Allele Identifier: CA376553255

Gene: RET

Linked Data

• ClinVar Variation Id: 1785415
• ClinVar RCV Id: RCV002422164
• dbSNP Id: rs2132852797
• gnomAD v4: 10-43114672-G-T
• MyVariant Identifiers: chr10:g.43610120G>T (hg19) ; chr10:g.43114672G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114672G>T , CM000672.2:g.43114672G>T	GRCh38
NC_000010.10:g.43610120G>T , CM000672.1:g.43610120G>T	GRCh37
NC_000010.9:g.42930126G>T	NCBI36
NG_007489.1:g.42604G>T , LRG_518:g.42604G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1676G>T	ENSP00000480088.2:p.Gly559Val
ENST00000683007.1:n.1646G>T
ENST00000683872.1:n.1637G>T
ENST00000340058.6:c.2072G>T	ENSP00000344798.4:p.Gly691Val
ENST00000355710.8:c.2072G>T MANE Select	ENSP00000347942.3:p.Gly691Val
ENST00000671844.1:c.*666G>T	ENSP00000500541.1:n.*666G>T
ENST00000672389.1:c.*666G>T	ENSP00000500252.1:n.*666G>T
ENST00000340058.5:c.2072G>T	ENSP00000344798.4:p.Gly691Val
ENST00000355710.7:c.2072G>T	ENSP00000347942.3:p.Gly691Val
ENST00000615310.4:c.1289+3440G>T	ENSP00000480088.1:n.1289+3440G>T
NM_020630.4:c.2072G>T , LRG_518t2:c.2072G>T	NP_065681.1:p.Gly691Val
NM_020975.4:c.2072G>T , LRG_518t1:c.2072G>T	NP_066124.1:p.Gly691Val
XM_011540027.1:c.2072G>T	XP_011538329.1:p.Gly691Val
NM_001355216.1:c.1310G>T	NP_001342145.1:p.Gly437Val
NM_020630.5:c.2072G>T	NP_065681.1:p.Gly691Val
NM_020975.5:c.2072G>T	NP_066124.1:p.Gly691Val
NM_020975.6:c.2072G>T MANE Select	NP_066124.1:p.Gly691Val
NM_020630.6:c.2072G>T	NP_065681.1:p.Gly691Val