Canonical Allele Identifier: CA376547533

Gene: RET

Linked Data

• ClinVar Variation Id: 543752
• ClinVar RCV Id: RCV000654591 ; RCV002360666 ; RCV002507129
• dbSNP Id: rs906695652
• gnomAD v2: 10-43604569-G-T
• gnomAD v4: 10-43109121-G-T
• MyVariant Identifiers: chr10:g.43604569G>T (hg19) ; chr10:g.43109121G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43109121G>T , CM000672.2:g.43109121G>T	GRCh38
NC_000010.10:g.43604569G>T , CM000672.1:g.43604569G>T	GRCh37
NC_000010.9:g.42924575G>T	NCBI36
NG_007489.1:g.37053G>T , LRG_518:g.37053G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.868-2086G>T	ENSP00000480088.2:n.868-2086G>T
ENST00000683007.1:n.728G>T
ENST00000340058.6:c.1154G>T	ENSP00000344798.4:p.Gly385Val
ENST00000355710.8:c.1154G>T MANE Select	ENSP00000347942.3:p.Gly385Val
ENST00000671844.1:c.626-2086G>T	ENSP00000500541.1:n.626-2086G>T
ENST00000672389.1:c.74-2086G>T	ENSP00000500252.1:n.74-2086G>T
ENST00000340058.5:c.1154G>T	ENSP00000344798.4:p.Gly385Val
ENST00000355710.7:c.1154G>T	ENSP00000347942.3:p.Gly385Val
ENST00000498820.5:c.74-2978G>T	ENSP00000419080.1:n.74-2978G>T
ENST00000615310.4:c.1154G>T	ENSP00000480088.1:p.Gly385Val
NM_020630.4:c.1154G>T , LRG_518t2:c.1154G>T	NP_065681.1:p.Gly385Val
NM_020975.4:c.1154G>T , LRG_518t1:c.1154G>T	NP_066124.1:p.Gly385Val
XM_011540027.1:c.1154G>T	XP_011538329.1:p.Gly385Val
NM_001355216.1:c.392G>T	NP_001342145.1:p.Gly131Val
NM_020630.5:c.1154G>T	NP_065681.1:p.Gly385Val
NM_020975.5:c.1154G>T	NP_066124.1:p.Gly385Val
NM_020975.6:c.1154G>T MANE Select	NP_066124.1:p.Gly385Val
NM_020630.6:c.1154G>T	NP_065681.1:p.Gly385Val