Canonical Allele Identifier: CA2608897171

Gene: RET

Linked Data

• gnomAD v4: 10-43130194-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130194A>G , CM000672.2:g.43130194A>G	GRCh38
NC_000010.10:g.43625642A>G , CM000672.1:g.43625642A>G	GRCh37
NC_000010.9:g.42945648A>G	NCBI36
NG_007489.1:g.58126A>G , LRG_518:g.58126A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*3440A>G	ENSP00000480088.2:n.*3440A>G
ENST00000683007.1:n.6233A>G
ENST00000355710.8:c.*1925A>G MANE Select	ENSP00000347942.3:n.*1925A>G
ENST00000355710.7:c.*1925A>G	ENSP00000347942.3:n.*1925A>G
ENST00000615310.4:c.*2619A>G	ENSP00000480088.1:n.*2619A>G
NM_020975.4:c.*1925A>G , LRG_518t1:c.*1925A>G	NP_066124.1:n.*1925A>G
XM_011540027.1:c.*693A>G	XP_011538329.1:n.*693A>G
NM_020975.5:c.*1925A>G	NP_066124.1:n.*1925A>G
NM_020975.6:c.*1925A>G MANE Select	NP_066124.1:n.*1925A>G