Canonical Allele Identifier: CA2574532177

Gene: RET

Linked Data

• ClinVar Variation Id: 2728221
• ClinVar RCV Id: RCV003531446
• gnomAD v4: 10-43119756-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119756A>G , CM000672.2:g.43119756A>G	GRCh38
NC_000010.10:g.43615204A>G , CM000672.1:g.43615204A>G	GRCh37
NC_000010.9:g.42935210A>G	NCBI36
NG_007489.1:g.47688A>G , LRG_518:g.47688A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+11A>G	ENSP00000480088.2:n.2211+11A>G
ENST00000683007.1:n.2181+11A>G
ENST00000683872.1:n.2172+11A>G
ENST00000340058.6:c.2607+11A>G	ENSP00000344798.4:n.2607+11A>G
ENST00000355710.8:c.2607+11A>G MANE Select	ENSP00000347942.3:n.2607+11A>G
ENST00000671844.1:c.*1201+11A>G	ENSP00000500541.1:n.*1201+11A>G
ENST00000672389.1:c.*1201+11A>G	ENSP00000500252.1:n.*1201+11A>G
ENST00000340058.5:c.2607+11A>G	ENSP00000344798.4:n.2607+11A>G
ENST00000355710.7:c.2607+11A>G	ENSP00000347942.3:n.2607+11A>G
ENST00000615310.4:c.1333+11A>G	ENSP00000480088.1:n.1333+11A>G
NM_020630.4:c.2607+11A>G , LRG_518t2:c.2607+11A>G	NP_065681.1:n.2607+11A>G
NM_020975.4:c.2607+11A>G , LRG_518t1:c.2607+11A>G	NP_066124.1:n.2607+11A>G
XM_011540027.1:c.2607+11A>G	XP_011538329.1:n.2607+11A>G
NM_001355216.1:c.1845+11A>G	NP_001342145.1:n.1845+11A>G
NM_020630.5:c.2607+11A>G	NP_065681.1:n.2607+11A>G
NM_020975.5:c.2607+11A>G	NP_066124.1:n.2607+11A>G
NM_020975.6:c.2607+11A>G MANE Select	NP_066124.1:n.2607+11A>G
NM_020630.6:c.2607+11A>G	NP_065681.1:n.2607+11A>G