Canonical Allele Identifier: CA1905814122

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077227_43077230delinsCCCT , CM000672.2:g.43077227_43077230delinsCCCT	GRCh38
NC_000010.10:g.43572675_43572678delinsCCCT , CM000672.1:g.43572675_43572678delinsCCCT	GRCh37
NC_000010.9:g.42892681_42892684delinsCCCT	NCBI36
NG_007489.1:g.5159_5162delinsCCCT , LRG_518:g.5159_5162delinsCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.-32_-29delinsCCCT	ENSP00000480088.2:n.-32_-29delinsCCCT
ENST00000340058.6:c.-32_-29delinsCCCT	ENSP00000344798.4:n.-32_-29delinsCCCT
ENST00000355710.8:c.-32_-29delinsCCCT MANE Select	ENSP00000347942.3:n.-32_-29delinsCCCT
ENST00000671844.1:c.-32_-29delinsCCCT	ENSP00000500541.1:n.-32_-29delinsCCCT
ENST00000672389.1:c.-32_-29delinsCCCT	ENSP00000500252.1:n.-32_-29delinsCCCT
ENST00000340058.5:c.-32_-29delinsCCCT	ENSP00000344798.4:n.-32_-29delinsCCCT
ENST00000355710.7:c.-32_-29delinsCCCT	ENSP00000347942.3:n.-32_-29delinsCCCT
ENST00000498820.5:c.-32_-29delinsCCCT	ENSP00000419080.1:n.-32_-29delinsCCCT
ENST00000615310.4:c.-32_-29delinsCCCT	ENSP00000480088.1:n.-32_-29delinsCCCT
NM_020630.4:c.-32_-29delinsCCCT , LRG_518t2:c.-32_-29delinsCCCT	NP_065681.1:n.-32_-29delinsCCCT
NM_020975.4:c.-32_-29delinsCCCT , LRG_518t1:c.-32_-29delinsCCCT	NP_066124.1:n.-32_-29delinsCCCT
XM_011540027.1:c.-32_-29delinsCCCT	XP_011538329.1:n.-32_-29delinsCCCT
NM_020630.5:c.-32_-29delinsCCCT	NP_065681.1:n.-32_-29delinsCCCT
NM_020975.5:c.-32_-29delinsCCCT	NP_066124.1:n.-32_-29delinsCCCT
NM_020975.6:c.-32_-29delinsCCCT MANE Select	NP_066124.1:n.-32_-29delinsCCCT
NM_020630.6:c.-32_-29delinsCCCT	NP_065681.1:n.-32_-29delinsCCCT