Canonical Allele Identifier: CA1905822074

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43121873_43121874delinsTG , CM000672.2:g.43121873_43121874delinsTG	GRCh38
NC_000010.10:g.43617321_43617322delinsTG , CM000672.1:g.43617321_43617322delinsTG	GRCh37
NC_000010.9:g.42937327_42937328delinsTG	NCBI36
NG_007489.1:g.49805_49806delinsTG , LRG_518:g.49805_49806delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2335-73_2335-72delinsTG	ENSP00000480088.2:n.2335-73_2335-72delinsTG
ENST00000683007.1:n.2305-73_2305-72delinsTG
ENST00000340058.6:c.2731-73_2731-72delinsTG	ENSP00000344798.4:n.2731-73_2731-72delinsTG
ENST00000355710.8:c.2731-73_2731-72delinsTG MANE Select	ENSP00000347942.3:n.2731-73_2731-72delinsTG
ENST00000671844.1:c.*1325-73_*1325-72delinsTG	ENSP00000500541.1:n.*1325-73_*1325-72delinsTG
ENST00000672389.1:c.*1325-73_*1325-72delinsTG	ENSP00000500252.1:n.*1325-73_*1325-72delinsTG
ENST00000340058.5:c.2731-73_2731-72delinsTG	ENSP00000344798.4:n.2731-73_2731-72delinsTG
ENST00000355710.7:c.2731-73_2731-72delinsTG	ENSP00000347942.3:n.2731-73_2731-72delinsTG
ENST00000615310.4:c.*80-73_*80-72delinsTG	ENSP00000480088.1:n.*80-73_*80-72delinsTG
NM_020630.4:c.2731-73_2731-72delinsTG , LRG_518t2:c.2731-73_2731-72delinsTG	NP_065681.1:n.2731-73_2731-72delinsTG
NM_020975.4:c.2731-73_2731-72delinsTG , LRG_518t1:c.2731-73_2731-72delinsTG	NP_066124.1:n.2731-73_2731-72delinsTG
XM_011540027.1:c.2731-73_2731-72delinsTG	XP_011538329.1:n.2731-73_2731-72delinsTG
NM_001355216.1:c.1969-73_1969-72delinsTG	NP_001342145.1:n.1969-73_1969-72delinsTG
NM_020630.5:c.2731-73_2731-72delinsTG	NP_065681.1:n.2731-73_2731-72delinsTG
NM_020975.5:c.2731-73_2731-72delinsTG	NP_066124.1:n.2731-73_2731-72delinsTG
NM_020975.6:c.2731-73_2731-72delinsTG MANE Select	NP_066124.1:n.2731-73_2731-72delinsTG
NM_020630.6:c.2731-73_2731-72delinsTG	NP_065681.1:n.2731-73_2731-72delinsTG