Canonical Allele Identifier: CA665319305

Gene: RET

Linked Data

• dbSNP Id: rs1302360312
• MyVariant Identifiers: chr10:g.43613458_43613459del (hg19) ; chr10:g.43118010_43118011del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118015_43118016del , CM000672.2:g.43118015_43118016del	GRCh38
NC_000010.10:g.43613463_43613464del , CM000672.1:g.43613463_43613464del	GRCh37
NC_000010.9:g.42933469_42933470del	NCBI36
NG_007489.1:g.45947_45948del , LRG_518:g.45947_45948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1889-358_1889-357del	ENSP00000480088.2:n.1889-358_1889-357del
ENST00000683007.1:n.1859-358_1859-357del
ENST00000683872.1:n.1850-358_1850-357del
ENST00000340058.6:c.2285-358_2285-357del	ENSP00000344798.4:n.2285-358_2285-357del
ENST00000355710.8:c.2285-358_2285-357del MANE Select	ENSP00000347942.3:n.2285-358_2285-357del
ENST00000671844.1:c.*879-358_*879-357del	ENSP00000500541.1:n.*879-358_*879-357del
ENST00000672389.1:c.*879-358_*879-357del	ENSP00000500252.1:n.*879-358_*879-357del
ENST00000340058.5:c.2285-358_2285-357del	ENSP00000344798.4:n.2285-358_2285-357del
ENST00000355710.7:c.2285-358_2285-357del	ENSP00000347942.3:n.2285-358_2285-357del
ENST00000615310.4:c.1290-1687_1290-1686del	ENSP00000480088.1:n.1290-1687_1290-1686del
NM_020630.4:c.2285-358_2285-357del , LRG_518t2:c.2285-358_2285-357del	NP_065681.1:n.2285-358_2285-357del
NM_020975.4:c.2285-358_2285-357del , LRG_518t1:c.2285-358_2285-357del	NP_066124.1:n.2285-358_2285-357del
XM_011540027.1:c.2285-358_2285-357del	XP_011538329.1:n.2285-358_2285-357del
NM_001355216.1:c.1523-358_1523-357del	NP_001342145.1:n.1523-358_1523-357del
NM_020630.5:c.2285-358_2285-357del	NP_065681.1:n.2285-358_2285-357del
NM_020975.5:c.2285-358_2285-357del	NP_066124.1:n.2285-358_2285-357del
NM_020975.6:c.2285-358_2285-357del MANE Select	NP_066124.1:n.2285-358_2285-357del
NM_020630.6:c.2285-358_2285-357del	NP_065681.1:n.2285-358_2285-357del