Canonical Allele Identifier: CA2721903614

Gene: RET

Linked Data

• dbSNP Id: rs2132840407

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114341del , CM000672.2:g.43114341del	GRCh38
NC_000010.10:g.43609789del , CM000672.1:g.43609789del	GRCh37
NC_000010.9:g.42929795del	NCBI36
NG_007489.1:g.42273del , LRG_518:g.42273del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1484-139del	ENSP00000480088.2:n.1484-139del
ENST00000683007.1:n.1454-139del
ENST00000683872.1:n.1306del
ENST00000340058.6:c.1880-139del	ENSP00000344798.4:n.1880-139del
ENST00000355710.8:c.1880-139del MANE Select	ENSP00000347942.3:n.1880-139del
ENST00000671844.1:c.*474-139del	ENSP00000500541.1:n.*474-139del
ENST00000672389.1:c.*474-139del	ENSP00000500252.1:n.*474-139del
ENST00000340058.5:c.1880-139del	ENSP00000344798.4:n.1880-139del
ENST00000355710.7:c.1880-139del	ENSP00000347942.3:n.1880-139del
ENST00000498820.5:c.431-139del	ENSP00000419080.1:n.431-139del
ENST00000615310.4:c.1289+3109del	ENSP00000480088.1:n.1289+3109del
NM_020630.4:c.1880-139del , LRG_518t2:c.1880-139del	NP_065681.1:n.1880-139del
NM_020975.4:c.1880-139del , LRG_518t1:c.1880-139del	NP_066124.1:n.1880-139del
XM_011540027.1:c.1880-139del	XP_011538329.1:n.1880-139del
NM_001355216.1:c.1118-139del	NP_001342145.1:n.1118-139del
NM_020630.5:c.1880-139del	NP_065681.1:n.1880-139del
NM_020975.5:c.1880-139del	NP_066124.1:n.1880-139del
NM_020975.6:c.1880-139del MANE Select	NP_066124.1:n.1880-139del
NM_020630.6:c.1880-139del	NP_065681.1:n.1880-139del