Canonical Allele Identifier: CA376770309

Gene: RET

Linked Data

• ClinVar Variation Id: 1462621
• ClinVar RCV Id: RCV001968569
• dbSNP Id: rs2132661188
• COSMIC: COSM4014149 ; COSM4014150
• MyVariant Identifiers: chr10:g.43596039G>A (hg19) ; chr10:g.43100591G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100591G>A , CM000672.2:g.43100591G>A	GRCh38
NC_000010.10:g.43596039G>A , CM000672.1:g.43596039G>A	GRCh37
NC_000010.9:g.42916045G>A	NCBI36
NG_007489.1:g.28523G>A , LRG_518:g.28523G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.206G>A	ENSP00000480088.2:p.Gly69Asp
ENST00000683278.1:c.108G>A
ENST00000684216.1:c.108G>A
ENST00000340058.6:c.206G>A	ENSP00000344798.4:p.Gly69Asp
ENST00000355710.8:c.206G>A MANE Select	ENSP00000347942.3:p.Gly69Asp
ENST00000638465.1:c.108G>A
ENST00000640619.1:c.108G>A
ENST00000671844.1:c.206G>A	ENSP00000500541.1:p.Gly69Asp
ENST00000672389.1:c.74-10616G>A	ENSP00000500252.1:n.74-10616G>A
ENST00000340058.5:c.206G>A	ENSP00000344798.4:p.Gly69Asp
ENST00000355710.7:c.206G>A	ENSP00000347942.3:p.Gly69Asp
ENST00000498820.5:c.74-11508G>A	ENSP00000419080.1:n.74-11508G>A
ENST00000615310.4:c.206G>A	ENSP00000480088.1:p.Gly69Asp
NM_020630.4:c.206G>A , LRG_518t2:c.206G>A	NP_065681.1:p.Gly69Asp
NM_020975.4:c.206G>A , LRG_518t1:c.206G>A	NP_066124.1:p.Gly69Asp
XM_011540027.1:c.206G>A	XP_011538329.1:p.Gly69Asp
NM_020630.5:c.206G>A	NP_065681.1:p.Gly69Asp
NM_020975.5:c.206G>A	NP_066124.1:p.Gly69Asp
NM_020975.6:c.206G>A MANE Select	NP_066124.1:p.Gly69Asp
NM_020630.6:c.206G>A	NP_065681.1:p.Gly69Asp