Canonical Allele Identifier: CA592898373

Gene: RET

Linked Data

• dbSNP Id: rs1239086192
• gnomAD v2: 10-43625633-G-A
• gnomAD v3: 10-43130185-G-A
• gnomAD v4: 10-43130185-G-A
• MyVariant Identifiers: chr10:g.43625633G>A (hg19) ; chr10:g.43130185G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130185G>A , CM000672.2:g.43130185G>A	GRCh38
NC_000010.10:g.43625633G>A , CM000672.1:g.43625633G>A	GRCh37
NC_000010.9:g.42945639G>A	NCBI36
NG_007489.1:g.58117G>A , LRG_518:g.58117G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*3431G>A	ENSP00000480088.2:n.*3431G>A
ENST00000683007.1:n.6224G>A
ENST00000355710.8:c.*1916G>A MANE Select	ENSP00000347942.3:n.*1916G>A
ENST00000355710.7:c.*1916G>A	ENSP00000347942.3:n.*1916G>A
ENST00000615310.4:c.*2610G>A	ENSP00000480088.1:n.*2610G>A
NM_020975.4:c.*1916G>A , LRG_518t1:c.*1916G>A	NP_066124.1:n.*1916G>A
XM_011540027.1:c.*684G>A	XP_011538329.1:n.*684G>A
NM_020975.5:c.*1916G>A	NP_066124.1:n.*1916G>A
NM_020975.6:c.*1916G>A MANE Select	NP_066124.1:n.*1916G>A