Canonical Allele Identifier: CA1905813056

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113625_43113652delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT , CM000672.2:g.43113625_43113652delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	GRCh38
NC_000010.10:g.43609073_43609100delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT , CM000672.1:g.43609073_43609100delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	GRCh37
NC_000010.9:g.42929079_42929106delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	NCBI36
NG_007489.1:g.41557_41584delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT , LRG_518:g.41557_41584delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1433_1460delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	ENSP00000480088.2:p.Asn478=
ENST00000683007.1:n.1403_1430delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT
ENST00000683872.1:n.590_617delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT
ENST00000340058.6:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	ENSP00000344798.4:p.Asn610=
ENST00000355710.8:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT MANE Select	ENSP00000347942.3:p.Asn610=
ENST00000671844.1:c.*423_*450delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	ENSP00000500541.1:n.*423_*450delinsACTGCT...
ENST00000672389.1:c.*423_*450delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	ENSP00000500252.1:n.*423_*450delinsACTGCT...
ENST00000340058.5:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	ENSP00000344798.4:p.Asn610=
ENST00000355710.7:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	ENSP00000347942.3:p.Asn610=
ENST00000498820.5:c.380_407delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	ENSP00000419080.1:p.Asn127=
ENST00000615310.4:c.1289+2393_1289+2420delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	ENSP00000480088.1:n.1289+2393_1289+2420de...
NM_020630.4:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT , LRG_518t2:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	NP_065681.1:p.Asn610=
NM_020975.4:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT , LRG_518t1:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	NP_066124.1:p.Asn610=
XM_011540027.1:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	XP_011538329.1:p.Asn610=
NM_001355216.1:c.1067_1094delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	NP_001342145.1:p.Asn356=
NM_020630.5:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	NP_065681.1:p.Asn610=
NM_020975.5:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	NP_066124.1:p.Asn610=
NM_020975.6:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT MANE Select	NP_066124.1:p.Asn610=
NM_020630.6:c.1829_1856delinsACTGCTTCCCTGAGGAGGAGAAGTGCTT	NP_065681.1:p.Asn610=