Canonical Allele Identifier: CA376770298

Gene: RET

Linked Data

• ClinVar Variation Id: 997535
• ClinVar RCV Id: RCV001292753
• dbSNP Id: rs749390385
• MyVariant Identifiers: chr10:g.43596032C>G (hg19) ; chr10:g.43100584C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100584C>G , CM000672.2:g.43100584C>G	GRCh38
NC_000010.10:g.43596032C>G , CM000672.1:g.43596032C>G	GRCh37
NC_000010.9:g.42916038C>G	NCBI36
NG_007489.1:g.28516C>G , LRG_518:g.28516C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.199C>G	ENSP00000480088.2:p.Arg67Gly
ENST00000683278.1:c.101C>G
ENST00000684216.1:c.101C>G
ENST00000340058.6:c.199C>G	ENSP00000344798.4:p.Arg67Gly
ENST00000355710.8:c.199C>G MANE Select	ENSP00000347942.3:p.Arg67Gly
ENST00000638465.1:c.101C>G
ENST00000640619.1:c.101C>G
ENST00000671844.1:c.199C>G	ENSP00000500541.1:p.Arg67Gly
ENST00000672389.1:c.74-10623C>G	ENSP00000500252.1:n.74-10623C>G
ENST00000340058.5:c.199C>G	ENSP00000344798.4:p.Arg67Gly
ENST00000355710.7:c.199C>G	ENSP00000347942.3:p.Arg67Gly
ENST00000498820.5:c.74-11515C>G	ENSP00000419080.1:n.74-11515C>G
ENST00000615310.4:c.199C>G	ENSP00000480088.1:p.Arg67Gly
NM_020630.4:c.199C>G , LRG_518t2:c.199C>G	NP_065681.1:p.Arg67Gly
NM_020975.4:c.199C>G , LRG_518t1:c.199C>G	NP_066124.1:p.Arg67Gly
XM_011540027.1:c.199C>G	XP_011538329.1:p.Arg67Gly
NM_020630.5:c.199C>G	NP_065681.1:p.Arg67Gly
NM_020975.5:c.199C>G	NP_066124.1:p.Arg67Gly
NM_020975.6:c.199C>G MANE Select	NP_066124.1:p.Arg67Gly
NM_020630.6:c.199C>G	NP_065681.1:p.Arg67Gly