Canonical Allele Identifier: CA665321870

Gene: RET

Linked Data

• dbSNP Id: rs1271239377
• MyVariant Identifiers: chr10:g.43595684_43595688del (hg19) ; chr10:g.43100236_43100240del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100236_43100240del , CM000672.2:g.43100236_43100240del	GRCh38
NC_000010.10:g.43595684_43595688del , CM000672.1:g.43595684_43595688del	GRCh37
NC_000010.9:g.42915690_42915694del	NCBI36
NG_007489.1:g.28168_28172del , LRG_518:g.28168_28172del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.74-223_74-219del	ENSP00000480088.2:n.74-223_74-219del
ENST00000340058.6:c.74-223_74-219del	ENSP00000344798.4:n.74-223_74-219del
ENST00000355710.8:c.74-223_74-219del MANE Select	ENSP00000347942.3:n.74-223_74-219del
ENST00000671844.1:c.74-223_74-219del	ENSP00000500541.1:n.74-223_74-219del
ENST00000672389.1:c.74-10971_74-10967del	ENSP00000500252.1:n.74-10971_74-10967del
ENST00000340058.5:c.74-223_74-219del	ENSP00000344798.4:n.74-223_74-219del
ENST00000355710.7:c.74-223_74-219del	ENSP00000347942.3:n.74-223_74-219del
ENST00000498820.5:c.74-11863_74-11859del	ENSP00000419080.1:n.74-11863_74-11859del
ENST00000615310.4:c.74-223_74-219del	ENSP00000480088.1:n.74-223_74-219del
NM_020630.4:c.74-223_74-219del , LRG_518t2:c.74-223_74-219del	NP_065681.1:n.74-223_74-219del
NM_020975.4:c.74-223_74-219del , LRG_518t1:c.74-223_74-219del	NP_066124.1:n.74-223_74-219del
XM_011540027.1:c.74-223_74-219del	XP_011538329.1:n.74-223_74-219del
NM_020630.5:c.74-223_74-219del	NP_065681.1:n.74-223_74-219del
NM_020975.5:c.74-223_74-219del	NP_066124.1:n.74-223_74-219del
NM_020975.6:c.74-223_74-219del MANE Select	NP_066124.1:n.74-223_74-219del
NM_020630.6:c.74-223_74-219del	NP_065681.1:n.74-223_74-219del