Canonical Allele Identifier: CA10635704

Gene: RET

Linked Data

• ClinVar Variation Id: 299883
• ClinVar RCV Id: RCV000291019 ; RCV000325032 ; RCV000383449 ; RCV000381849
• dbSNP Id: rs886046983
• gnomAD v4: 10-43077072-C-A
• MyVariant Identifiers: chr10:g.43572520C>A (hg19) ; chr10:g.43077072C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077072C>A , CM000672.2:g.43077072C>A	GRCh38
NC_000010.10:g.43572520C>A , CM000672.1:g.43572520C>A	GRCh37
NC_000010.9:g.42892526C>A	NCBI36
NG_007489.1:g.5004C>A , LRG_518:g.5004C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340058.6:c.-187C>A	ENSP00000344798.4:n.-187C>A
ENST00000355710.8:c.-187C>A MANE Select	ENSP00000347942.3:n.-187C>A
ENST00000671844.1:c.-187C>A	ENSP00000500541.1:n.-187C>A
ENST00000672389.1:c.-187C>A	ENSP00000500252.1:n.-187C>A
ENST00000355710.7:c.-187C>A	ENSP00000347942.3:n.-187C>A
ENST00000615310.4:c.-187C>A	ENSP00000480088.1:n.-187C>A
NM_020630.4:c.-187C>A , LRG_518t2:c.-187C>A	NP_065681.1:n.-187C>A
NM_020975.4:c.-187C>A , LRG_518t1:c.-187C>A	NP_066124.1:n.-187C>A
XM_011540027.1:c.-187C>A	XP_011538329.1:n.-187C>A
NM_020630.5:c.-187C>A	NP_065681.1:n.-187C>A
NM_020975.5:c.-187C>A	NP_066124.1:n.-187C>A
NM_020975.6:c.-187C>A MANE Select	NP_066124.1:n.-187C>A
NM_020630.6:c.-187C>A	NP_065681.1:n.-187C>A