Canonical Allele Identifier: CA376552778

Gene: RET

Linked Data

• dbSNP Id: rs2132829914
• MyVariant Identifiers: chr10:g.43609081C>A (hg19) ; chr10:g.43113633C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113633C>A , CM000672.2:g.43113633C>A	GRCh38
NC_000010.10:g.43609081C>A , CM000672.1:g.43609081C>A	GRCh37
NC_000010.9:g.42929087C>A	NCBI36
NG_007489.1:g.41565C>A , LRG_518:g.41565C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1441C>A	ENSP00000480088.2:p.Pro481Thr
ENST00000683007.1:n.1411C>A
ENST00000683872.1:n.598C>A
ENST00000340058.6:c.1837C>A	ENSP00000344798.4:p.Pro613Thr
ENST00000355710.8:c.1837C>A MANE Select	ENSP00000347942.3:p.Pro613Thr
ENST00000671844.1:c.*431C>A	ENSP00000500541.1:n.*431C>A
ENST00000672389.1:c.*431C>A	ENSP00000500252.1:n.*431C>A
ENST00000340058.5:c.1837C>A	ENSP00000344798.4:p.Pro613Thr
ENST00000355710.7:c.1837C>A	ENSP00000347942.3:p.Pro613Thr
ENST00000498820.5:c.388C>A	ENSP00000419080.1:p.Pro130Thr
ENST00000615310.4:c.1289+2401C>A	ENSP00000480088.1:n.1289+2401C>A
NM_020630.4:c.1837C>A , LRG_518t2:c.1837C>A	NP_065681.1:p.Pro613Thr
NM_020975.4:c.1837C>A , LRG_518t1:c.1837C>A	NP_066124.1:p.Pro613Thr
XM_011540027.1:c.1837C>A	XP_011538329.1:p.Pro613Thr
NM_001355216.1:c.1075C>A	NP_001342145.1:p.Pro359Thr
NM_020630.5:c.1837C>A	NP_065681.1:p.Pro613Thr
NM_020975.5:c.1837C>A	NP_066124.1:p.Pro613Thr
NM_020975.6:c.1837C>A MANE Select	NP_066124.1:p.Pro613Thr
NM_020630.6:c.1837C>A	NP_065681.1:p.Pro613Thr