Canonical Allele Identifier: CA665316808

Gene: RET

Linked Data

• dbSNP Id: rs1340306491
• gnomAD v3: 10-43130247-G-A
• gnomAD v4: 10-43130247-G-A
• MyVariant Identifiers: chr10:g.43625695G>A (hg19) ; chr10:g.43130247G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130247G>A , CM000672.2:g.43130247G>A	GRCh38
NC_000010.10:g.43625695G>A , CM000672.1:g.43625695G>A	GRCh37
NC_000010.9:g.42945701G>A	NCBI36
NG_007489.1:g.58179G>A , LRG_518:g.58179G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*3493G>A	ENSP00000480088.2:n.*3493G>A
ENST00000683007.1:n.6286G>A
ENST00000355710.8:c.*1978G>A MANE Select	ENSP00000347942.3:n.*1978G>A
ENST00000355710.7:c.*1978G>A	ENSP00000347942.3:n.*1978G>A
ENST00000615310.4:c.*2672G>A	ENSP00000480088.1:n.*2672G>A
NM_020975.4:c.*1978G>A , LRG_518t1:c.*1978G>A	NP_066124.1:n.*1978G>A
XM_011540027.1:c.*746G>A	XP_011538329.1:n.*746G>A
NM_020975.5:c.*1978G>A	NP_066124.1:n.*1978G>A
NM_020975.6:c.*1978G>A MANE Select	NP_066124.1:n.*1978G>A