Canonical Allele Identifier: CA009343

Gene: RET

Linked Data

• ClinVar Variation Id: 136124
• ClinVar RCV Id: RCV000123326 ; RCV001026582 ; RCV003467096
• dbSNP Id: rs587780816
• gnomAD v4: 10-43105083-G-A
• MyVariant Identifiers: chr10:g.43600531G>A (hg19) ; chr10:g.43105083G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43105083G>A , CM000672.2:g.43105083G>A	GRCh38
NC_000010.10:g.43600531G>A , CM000672.1:g.43600531G>A	GRCh37
NC_000010.9:g.42920537G>A	NCBI36
NG_007489.1:g.33015G>A , LRG_518:g.33015G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.757G>A	ENSP00000480088.2:p.Val253Met
ENST00000683007.1:n.331G>A
ENST00000340058.6:c.757G>A	ENSP00000344798.4:p.Val253Met
ENST00000355710.8:c.757G>A MANE Select	ENSP00000347942.3:p.Val253Met
ENST00000671844.1:c.625+2454G>A	ENSP00000500541.1:n.625+2454G>A
ENST00000672389.1:c.74-6124G>A	ENSP00000500252.1:n.74-6124G>A
ENST00000340058.5:c.757G>A	ENSP00000344798.4:p.Val253Met
ENST00000355710.7:c.757G>A	ENSP00000347942.3:p.Val253Met
ENST00000479913.1:n.352G>A
ENST00000498820.5:c.74-7016G>A	ENSP00000419080.1:n.74-7016G>A
ENST00000615310.4:c.757G>A	ENSP00000480088.1:p.Val253Met
NM_020630.4:c.757G>A , LRG_518t2:c.757G>A	NP_065681.1:p.Val253Met
NM_020975.4:c.757G>A , LRG_518t1:c.757G>A	NP_066124.1:p.Val253Met
XM_011540027.1:c.757G>A	XP_011538329.1:p.Val253Met
NM_001355216.1:c.-6G>A	NP_001342145.1:n.-6G>A
NM_020630.5:c.757G>A	NP_065681.1:p.Val253Met
NM_020975.5:c.757G>A	NP_066124.1:p.Val253Met
NM_020975.6:c.757G>A MANE Select	NP_066124.1:p.Val253Met
NM_020630.6:c.757G>A	NP_065681.1:p.Val253Met