Canonical Allele Identifier: CA10576788

Gene: RET

Linked Data

• ClinVar Variation Id: 229201
• ClinVar RCV Id: RCV000572702 ; RCV002503860 ; RCV004532763 ; RCV000221356 ; RCV001580474
• dbSNP Id: rs876657980
• gnomAD v2: 10-43572705-C-A
• gnomAD v3: 10-43077257-C-A
• gnomAD v4: 10-43077257-C-A
• MyVariant Identifiers: chr10:g.43572705C>A (hg19) ; chr10:g.43077257C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077257C>A , CM000672.2:g.43077257C>A	GRCh38
NC_000010.10:g.43572705C>A , CM000672.1:g.43572705C>A	GRCh37
NC_000010.9:g.42892711C>A	NCBI36
NG_007489.1:g.5189C>A , LRG_518:g.5189C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.-2C>A	ENSP00000480088.2:n.-2C>A
ENST00000340058.6:c.-2C>A	ENSP00000344798.4:n.-2C>A
ENST00000355710.8:c.-2C>A MANE Select	ENSP00000347942.3:n.-2C>A
ENST00000671844.1:c.-2C>A	ENSP00000500541.1:n.-2C>A
ENST00000672389.1:c.-2C>A	ENSP00000500252.1:n.-2C>A
ENST00000340058.5:c.-2C>A	ENSP00000344798.4:n.-2C>A
ENST00000355710.7:c.-2C>A	ENSP00000347942.3:n.-2C>A
ENST00000498820.5:c.-2C>A	ENSP00000419080.1:n.-2C>A
ENST00000615310.4:c.-2C>A	ENSP00000480088.1:n.-2C>A
NM_020630.4:c.-2C>A , LRG_518t2:c.-2C>A	NP_065681.1:n.-2C>A
NM_020975.4:c.-2C>A , LRG_518t1:c.-2C>A	NP_066124.1:n.-2C>A
XM_011540027.1:c.-2C>A	XP_011538329.1:n.-2C>A
NM_020630.5:c.-2C>A	NP_065681.1:n.-2C>A
NM_020975.5:c.-2C>A	NP_066124.1:n.-2C>A
NM_020975.6:c.-2C>A MANE Select	NP_066124.1:n.-2C>A
NM_020630.6:c.-2C>A	NP_065681.1:n.-2C>A