Canonical Allele Identifier: CA1905814362

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077413_43077417delinsCCTTT , CM000672.2:g.43077413_43077417delinsCCTTT	GRCh38
NC_000010.10:g.43572861_43572865delinsCCTTT , CM000672.1:g.43572861_43572865delinsCCTTT	GRCh37
NC_000010.9:g.42892867_42892871delinsCCTTT	NCBI36
NG_007489.1:g.5345_5349delinsCCTTT , LRG_518:g.5345_5349delinsCCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.73+82_73+86delinsCCTTT	ENSP00000480088.2:n.73+82_73+86delinsCCTTT
ENST00000340058.6:c.73+82_73+86delinsCCTTT	ENSP00000344798.4:n.73+82_73+86delinsCCTTT
ENST00000355710.8:c.73+82_73+86delinsCCTTT MANE Select	ENSP00000347942.3:n.73+82_73+86delinsCCTTT
ENST00000671844.1:c.73+82_73+86delinsCCTTT	ENSP00000500541.1:n.73+82_73+86delinsCCTTT
ENST00000672389.1:c.73+82_73+86delinsCCTTT	ENSP00000500252.1:n.73+82_73+86delinsCCTTT
ENST00000340058.5:c.73+82_73+86delinsCCTTT	ENSP00000344798.4:n.73+82_73+86delinsCCTTT
ENST00000355710.7:c.73+82_73+86delinsCCTTT	ENSP00000347942.3:n.73+82_73+86delinsCCTTT
ENST00000498820.5:c.73+82_73+86delinsCCTTT	ENSP00000419080.1:n.73+82_73+86delinsCCTTT
ENST00000615310.4:c.73+82_73+86delinsCCTTT	ENSP00000480088.1:n.73+82_73+86delinsCCTTT
NM_020630.4:c.73+82_73+86delinsCCTTT , LRG_518t2:c.73+82_73+86delinsCCTTT	NP_065681.1:n.73+82_73+86delinsCCTTT
NM_020975.4:c.73+82_73+86delinsCCTTT , LRG_518t1:c.73+82_73+86delinsCCTTT	NP_066124.1:n.73+82_73+86delinsCCTTT
XM_011540027.1:c.73+82_73+86delinsCCTTT	XP_011538329.1:n.73+82_73+86delinsCCTTT
NM_020630.5:c.73+82_73+86delinsCCTTT	NP_065681.1:n.73+82_73+86delinsCCTTT
NM_020975.5:c.73+82_73+86delinsCCTTT	NP_066124.1:n.73+82_73+86delinsCCTTT
NM_020975.6:c.73+82_73+86delinsCCTTT MANE Select	NP_066124.1:n.73+82_73+86delinsCCTTT
NM_020630.6:c.73+82_73+86delinsCCTTT	NP_065681.1:n.73+82_73+86delinsCCTTT