Canonical Allele Identifier: CA2830563755

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120120_43120121delinsTA , CM000672.2:g.43120120_43120121delinsTA	GRCh38
NC_000010.10:g.43615568_43615569delinsTA , CM000672.1:g.43615568_43615569delinsTA	GRCh37
NC_000010.9:g.42935574_42935575delinsTA	NCBI36
NG_007489.1:g.48052_48053delinsTA , LRG_518:g.48052_48053delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2251_2252delinsTA	ENSP00000480088.2:p.Ala751Tyr
ENST00000683007.1:n.2221_2222delinsTA
ENST00000683872.1:n.2212_2213delinsTA
ENST00000340058.6:c.2647_2648delinsTA	ENSP00000344798.4:p.Ala883Tyr
ENST00000355710.8:c.2647_2648delinsTA MANE Select	ENSP00000347942.3:p.Ala883Tyr
ENST00000671844.1:c.*1241_*1242delinsTA	ENSP00000500541.1:n.*1241_*1242delinsTA
ENST00000672389.1:c.*1241_*1242delinsTA	ENSP00000500252.1:n.*1241_*1242delinsTA
ENST00000340058.5:c.2647_2648delinsTA	ENSP00000344798.4:p.Ala883Tyr
ENST00000355710.7:c.2647_2648delinsTA	ENSP00000347942.3:p.Ala883Tyr
ENST00000615310.4:c.1373_1374delinsTA	ENSP00000480088.1:p.Ser458Ile
NM_020630.4:c.2647_2648delinsTA , LRG_518t2:c.2647_2648delinsTA	NP_065681.1:p.Ala883Tyr
NM_020975.4:c.2647_2648delinsTA , LRG_518t1:c.2647_2648delinsTA	NP_066124.1:p.Ala883Tyr
XM_011540027.1:c.2647_2648delinsTA	XP_011538329.1:p.Ala883Tyr
NM_001355216.1:c.1885_1886delinsTA	NP_001342145.1:p.Ala629Tyr
NM_020630.5:c.2647_2648delinsTA	NP_065681.1:p.Ala883Tyr
NM_020975.5:c.2647_2648delinsTA	NP_066124.1:p.Ala883Tyr
NM_020975.6:c.2647_2648delinsTA MANE Select	NP_066124.1:p.Ala883Tyr
NM_020630.6:c.2647_2648delinsTA	NP_065681.1:p.Ala883Tyr