Canonical Allele Identifier: CA2695211980

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118421del , CM000672.2:g.43118421del	GRCh38
NC_000010.10:g.43613869del , CM000672.1:g.43613869del	GRCh37
NC_000010.9:g.42933875del	NCBI36
NG_007489.1:g.46353del , LRG_518:g.46353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1937del	ENSP00000480088.2:p.Val646AlafsTer2
ENST00000683007.1:n.1907del
ENST00000683872.1:n.1898del
ENST00000340058.6:c.2333del	ENSP00000344798.4:p.Val778AlafsTer2
ENST00000355710.8:c.2333del MANE Select	ENSP00000347942.3:p.Val778AlafsTer2
ENST00000671844.1:c.*927del	ENSP00000500541.1:n.*927del
ENST00000672389.1:c.*927del	ENSP00000500252.1:n.*927del
ENST00000340058.5:c.2333del	ENSP00000344798.4:p.Val778AlafsTer2
ENST00000355710.7:c.2333del	ENSP00000347942.3:p.Val778AlafsTer2
ENST00000615310.4:c.1290-1281del	ENSP00000480088.1:n.1290-1281del
NM_020630.4:c.2333del , LRG_518t2:c.2333del	NP_065681.1:p.Val778AlafsTer2
NM_020975.4:c.2333del , LRG_518t1:c.2333del	NP_066124.1:p.Val778AlafsTer2
XM_011540027.1:c.2333del	XP_011538329.1:p.Val778AlafsTer2
NM_001355216.1:c.1571del	NP_001342145.1:p.Val524AlafsTer2
NM_020630.5:c.2333del	NP_065681.1:p.Val778AlafsTer2
NM_020975.5:c.2333del	NP_066124.1:p.Val778AlafsTer2
NM_020975.6:c.2333del MANE Select	NP_066124.1:p.Val778AlafsTer2
NM_020630.6:c.2333del	NP_065681.1:p.Val778AlafsTer2