Canonical Allele Identifier: CA035963

Gene: RET

Linked Data

• ClinVar Variation Id: 299895
• ClinVar RCV Id: RCV000295350 ; RCV000345576 ; RCV000381315 ; RCV000389662 ; RCV000662734 ; RCV001850584
• dbSNP Id: rs532810255
• ExAC: 10:43609137 G / A
• gnomAD v2: 10-43609137-G-A
• gnomAD v3: 10-43113689-G-A
• gnomAD v4: 10-43113689-G-A
• MyVariant Identifiers: chr10:g.43609137G>A (hg19) ; chr10:g.43113689G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113689G>A , CM000672.2:g.43113689G>A	GRCh38
NC_000010.10:g.43609137G>A , CM000672.1:g.43609137G>A	GRCh37
NC_000010.9:g.42929143G>A	NCBI36
NG_007489.1:g.41621G>A , LRG_518:g.41621G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1483+14G>A	ENSP00000480088.2:n.1483+14G>A
ENST00000683007.1:n.1453+14G>A
ENST00000683872.1:n.654G>A
ENST00000340058.6:c.1879+14G>A	ENSP00000344798.4:n.1879+14G>A
ENST00000355710.8:c.1879+14G>A MANE Select	ENSP00000347942.3:n.1879+14G>A
ENST00000671844.1:c.*473+14G>A	ENSP00000500541.1:n.*473+14G>A
ENST00000672389.1:c.*473+14G>A	ENSP00000500252.1:n.*473+14G>A
ENST00000340058.5:c.1879+14G>A	ENSP00000344798.4:n.1879+14G>A
ENST00000355710.7:c.1879+14G>A	ENSP00000347942.3:n.1879+14G>A
ENST00000498820.5:c.430+14G>A	ENSP00000419080.1:n.430+14G>A
ENST00000615310.4:c.1289+2457G>A	ENSP00000480088.1:n.1289+2457G>A
NM_020630.4:c.1879+14G>A , LRG_518t2:c.1879+14G>A	NP_065681.1:n.1879+14G>A
NM_020975.4:c.1879+14G>A , LRG_518t1:c.1879+14G>A	NP_066124.1:n.1879+14G>A
XM_011540027.1:c.1879+14G>A	XP_011538329.1:n.1879+14G>A
NM_001355216.1:c.1117+14G>A	NP_001342145.1:n.1117+14G>A
NM_020630.5:c.1879+14G>A	NP_065681.1:n.1879+14G>A
NM_020975.5:c.1879+14G>A	NP_066124.1:n.1879+14G>A
NM_020975.6:c.1879+14G>A MANE Select	NP_066124.1:n.1879+14G>A
NM_020630.6:c.1879+14G>A	NP_065681.1:n.1879+14G>A