Canonical Allele Identifier: CA1905819526

Gene: RET

Linked Data

• dbSNP Id: rs1838166818

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119779del , CM000672.2:g.43119779del	GRCh38
NC_000010.10:g.43615227del , CM000672.1:g.43615227del	GRCh37
NC_000010.9:g.42935233del	NCBI36
NG_007489.1:g.47711del , LRG_518:g.47711del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+34del	ENSP00000480088.2:n.2211+34del
ENST00000683007.1:n.2181+34del
ENST00000683872.1:n.2172+34del
ENST00000340058.6:c.2607+34del	ENSP00000344798.4:n.2607+34del
ENST00000355710.8:c.2607+34del MANE Select	ENSP00000347942.3:n.2607+34del
ENST00000671844.1:c.*1201+34del	ENSP00000500541.1:n.*1201+34del
ENST00000672389.1:c.*1201+34del	ENSP00000500252.1:n.*1201+34del
ENST00000340058.5:c.2607+34del	ENSP00000344798.4:n.2607+34del
ENST00000355710.7:c.2607+34del	ENSP00000347942.3:n.2607+34del
ENST00000615310.4:c.1333+34del	ENSP00000480088.1:n.1333+34del
NM_020630.4:c.2607+34del , LRG_518t2:c.2607+34del	NP_065681.1:n.2607+34del
NM_020975.4:c.2607+34del , LRG_518t1:c.2607+34del	NP_066124.1:n.2607+34del
XM_011540027.1:c.2607+34del	XP_011538329.1:n.2607+34del
NM_001355216.1:c.1845+34del	NP_001342145.1:n.1845+34del
NM_020630.5:c.2607+34del	NP_065681.1:n.2607+34del
NM_020975.5:c.2607+34del	NP_066124.1:n.2607+34del
NM_020975.6:c.2607+34del MANE Select	NP_066124.1:n.2607+34del
NM_020630.6:c.2607+34del	NP_065681.1:n.2607+34del