Canonical Allele Identifier: CA376552780

Gene: RET

Linked Data

• dbSNP Id: rs2132829914
• COSMIC: COSM4989959 ; COSM4989960
• MyVariant Identifiers: chr10:g.43609081C>T (hg19) ; chr10:g.43113633C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1441C>T	ENSP00000480088.2:p.Pro481Ser
ENST00000683007.1:n.1411C>T
ENST00000683872.1:n.598C>T
ENST00000340058.6:c.1837C>T	ENSP00000344798.4:p.Pro613Ser
ENST00000355710.8:c.1837C>T MANE Select	ENSP00000347942.3:p.Pro613Ser
ENST00000671844.1:c.*431C>T	ENSP00000500541.1:n.*431C>T
ENST00000672389.1:c.*431C>T	ENSP00000500252.1:n.*431C>T
ENST00000340058.5:c.1837C>T	ENSP00000344798.4:p.Pro613Ser
ENST00000355710.7:c.1837C>T	ENSP00000347942.3:p.Pro613Ser
ENST00000498820.5:c.388C>T	ENSP00000419080.1:p.Pro130Ser
ENST00000615310.4:c.1289+2401C>T	ENSP00000480088.1:n.1289+2401C>T
NM_020630.4:c.1837C>T , LRG_518t2:c.1837C>T	NP_065681.1:p.Pro613Ser
NM_020975.4:c.1837C>T , LRG_518t1:c.1837C>T	NP_066124.1:p.Pro613Ser
XM_011540027.1:c.1837C>T	XP_011538329.1:p.Pro613Ser
NM_001355216.1:c.1075C>T	NP_001342145.1:p.Pro359Ser
NM_020630.5:c.1837C>T	NP_065681.1:p.Pro613Ser
NM_020975.5:c.1837C>T	NP_066124.1:p.Pro613Ser
NM_020975.6:c.1837C>T MANE Select	NP_066124.1:p.Pro613Ser
NM_020630.6:c.1837C>T	NP_065681.1:p.Pro613Ser