Canonical Allele Identifier: CA376555872

Gene: RET

Linked Data

• ClinVar Variation Id: 1479171
• ClinVar RCV Id: RCV001976647 ; RCV002458927
• dbSNP Id: rs77724903
• gnomAD v2: 10-43613908-A-G
• gnomAD v4: 10-43118460-A-G
• MyVariant Identifiers: chr10:g.43613908A>G (hg19) ; chr10:g.43118460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118460A>G , CM000672.2:g.43118460A>G	GRCh38
NC_000010.10:g.43613908A>G , CM000672.1:g.43613908A>G	GRCh37
NC_000010.9:g.42933914A>G	NCBI36
NG_007489.1:g.46392A>G , LRG_518:g.46392A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1976A>G	ENSP00000480088.2:p.Tyr659Cys
ENST00000683007.1:n.1946A>G
ENST00000683872.1:n.1937A>G
ENST00000340058.6:c.2372A>G	ENSP00000344798.4:p.Tyr791Cys
ENST00000355710.8:c.2372A>G MANE Select	ENSP00000347942.3:p.Tyr791Cys
ENST00000671844.1:c.*966A>G	ENSP00000500541.1:n.*966A>G
ENST00000672389.1:c.*966A>G	ENSP00000500252.1:n.*966A>G
ENST00000340058.5:c.2372A>G	ENSP00000344798.4:p.Tyr791Cys
ENST00000355710.7:c.2372A>G	ENSP00000347942.3:p.Tyr791Cys
ENST00000615310.4:c.1290-1242A>G	ENSP00000480088.1:n.1290-1242A>G
NM_020630.4:c.2372A>G , LRG_518t2:c.2372A>G	NP_065681.1:p.Tyr791Cys
NM_020975.4:c.2372A>G , LRG_518t1:c.2372A>G	NP_066124.1:p.Tyr791Cys
XM_011540027.1:c.2372A>G	XP_011538329.1:p.Tyr791Cys
NM_001355216.1:c.1610A>G	NP_001342145.1:p.Tyr537Cys
NM_020630.5:c.2372A>G	NP_065681.1:p.Tyr791Cys
NM_020975.5:c.2372A>G	NP_066124.1:p.Tyr791Cys
NM_020975.6:c.2372A>G MANE Select	NP_066124.1:p.Tyr791Cys
NM_020630.6:c.2372A>G	NP_065681.1:p.Tyr791Cys