Canonical Allele Identifier: CA206267141

Gene: RET

Linked Data

• dbSNP Id: rs1054155175
• gnomAD v3: 10-43121850-A-G
• gnomAD v4: 10-43121850-A-G
• MyVariant Identifiers: chr10:g.43617298A>G (hg19) ; chr10:g.43121850A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43121850A>G , CM000672.2:g.43121850A>G	GRCh38
NC_000010.10:g.43617298A>G , CM000672.1:g.43617298A>G	GRCh37
NC_000010.9:g.42937304A>G	NCBI36
NG_007489.1:g.49782A>G , LRG_518:g.49782A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2335-96A>G	ENSP00000480088.2:n.2335-96A>G
ENST00000683007.1:n.2305-96A>G
ENST00000340058.6:c.2731-96A>G	ENSP00000344798.4:n.2731-96A>G
ENST00000355710.8:c.2731-96A>G MANE Select	ENSP00000347942.3:n.2731-96A>G
ENST00000671844.1:c.*1325-96A>G	ENSP00000500541.1:n.*1325-96A>G
ENST00000672389.1:c.*1325-96A>G	ENSP00000500252.1:n.*1325-96A>G
ENST00000340058.5:c.2731-96A>G	ENSP00000344798.4:n.2731-96A>G
ENST00000355710.7:c.2731-96A>G	ENSP00000347942.3:n.2731-96A>G
ENST00000615310.4:c.*80-96A>G	ENSP00000480088.1:n.*80-96A>G
NM_020630.4:c.2731-96A>G , LRG_518t2:c.2731-96A>G	NP_065681.1:n.2731-96A>G
NM_020975.4:c.2731-96A>G , LRG_518t1:c.2731-96A>G	NP_066124.1:n.2731-96A>G
XM_011540027.1:c.2731-96A>G	XP_011538329.1:n.2731-96A>G
NM_001355216.1:c.1969-96A>G	NP_001342145.1:n.1969-96A>G
NM_020630.5:c.2731-96A>G	NP_065681.1:n.2731-96A>G
NM_020975.5:c.2731-96A>G	NP_066124.1:n.2731-96A>G
NM_020975.6:c.2731-96A>G MANE Select	NP_066124.1:n.2731-96A>G
NM_020630.6:c.2731-96A>G	NP_065681.1:n.2731-96A>G