Canonical Allele Identifier: CA10635722

Gene: RET

Linked Data

• ClinVar Variation Id: 299899
• ClinVar RCV Id: RCV000375295 ; RCV000316068 ; RCV000279714 ; RCV000378390 ; RCV001428203 ; RCV002429252
• dbSNP Id: rs886046988
• gnomAD v2: 10-43615166-G-A
• gnomAD v4: 10-43119718-G-A
• MyVariant Identifiers: chr10:g.43615166G>A (hg19) ; chr10:g.43119718G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119718G>A , CM000672.2:g.43119718G>A	GRCh38
NC_000010.10:g.43615166G>A , CM000672.1:g.43615166G>A	GRCh37
NC_000010.9:g.42935172G>A	NCBI36
NG_007489.1:g.47650G>A , LRG_518:g.47650G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2184G>A	ENSP00000480088.2:p.Gln728=
ENST00000683007.1:n.2154G>A
ENST00000683872.1:n.2145G>A
ENST00000340058.6:c.2580G>A	ENSP00000344798.4:p.Gln860=
ENST00000355710.8:c.2580G>A MANE Select	ENSP00000347942.3:p.Gln860=
ENST00000671844.1:c.*1174G>A	ENSP00000500541.1:n.*1174G>A
ENST00000672389.1:c.*1174G>A	ENSP00000500252.1:n.*1174G>A
ENST00000340058.5:c.2580G>A	ENSP00000344798.4:p.Gln860=
ENST00000355710.7:c.2580G>A	ENSP00000347942.3:p.Gln860=
ENST00000615310.4:c.1306G>A	ENSP00000480088.1:p.Gly436Arg
NM_020630.4:c.2580G>A , LRG_518t2:c.2580G>A	NP_065681.1:p.Gln860=
NM_020975.4:c.2580G>A , LRG_518t1:c.2580G>A	NP_066124.1:p.Gln860=
XM_011540027.1:c.2580G>A	XP_011538329.1:p.Gln860=
NM_001355216.1:c.1818G>A	NP_001342145.1:p.Gln606=
NM_020630.5:c.2580G>A	NP_065681.1:p.Gln860=
NM_020975.5:c.2580G>A	NP_066124.1:p.Gln860=
NM_020975.6:c.2580G>A MANE Select	NP_066124.1:p.Gln860=
NM_020630.6:c.2580G>A	NP_065681.1:p.Gln860=