Canonical Allele Identifier: CA1905819539

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119786_43119816delinsGCCACACCCTGACCCACCACGCCCCTGCCAC , CM000672.2:g.43119786_43119816delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	GRCh38
NC_000010.10:g.43615234_43615264delinsGCCACACCCTGACCCACCACGCCCCTGCCAC , CM000672.1:g.43615234_43615264delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	GRCh37
NC_000010.9:g.42935240_42935270delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	NCBI36
NG_007489.1:g.47718_47748delinsGCCACACCCTGACCCACCACGCCCCTGCCAC , LRG_518:g.47718_47748delinsGCCACACCCTGACCCACCACGCCCCTGCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+41_2211+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	ENSP00000480088.2:n.2211+41_2211+71delinsGCCACACCCTGACCCACCAC...
ENST00000683007.1:n.2181+41_2181+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC
ENST00000683872.1:n.2172+41_2172+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC
ENST00000340058.6:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	ENSP00000344798.4:n.2607+41_2607+71delinsGCCACACCCTGACCCACCAC...
ENST00000355710.8:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC MANE Select	ENSP00000347942.3:n.2607+41_2607+71delinsGCCACACCCTGACCCACCAC...
ENST00000671844.1:c.*1201+41_*1201+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	ENSP00000500541.1:n.*1201+41_*1201+71delinsGCCACACCCTGACCCACC...
ENST00000672389.1:c.*1201+41_*1201+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	ENSP00000500252.1:n.*1201+41_*1201+71delinsGCCACACCCTGACCCACC...
ENST00000340058.5:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	ENSP00000344798.4:n.2607+41_2607+71delinsGCCACACCCTGACCCACCAC...
ENST00000355710.7:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	ENSP00000347942.3:n.2607+41_2607+71delinsGCCACACCCTGACCCACCAC...
ENST00000615310.4:c.1333+41_1333+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	ENSP00000480088.1:n.1333+41_1333+71delinsGCCACACCCTGACCCACCAC...
NM_020630.4:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC , LRG_518t2:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	NP_065681.1:n.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCT...
NM_020975.4:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC , LRG_518t1:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	NP_066124.1:n.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCT...
XM_011540027.1:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	XP_011538329.1:n.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCC...
NM_001355216.1:c.1845+41_1845+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	NP_001342145.1:n.1845+41_1845+71delinsGCCACACCCTGACCCACCACGCC...
NM_020630.5:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	NP_065681.1:n.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCT...
NM_020975.5:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	NP_066124.1:n.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCT...
NM_020975.6:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC MANE Select	NP_066124.1:n.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCT...
NM_020630.6:c.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCTGCCAC	NP_065681.1:n.2607+41_2607+71delinsGCCACACCCTGACCCACCACGCCCCT...