Canonical Allele Identifier: CA1905819412

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119721_43119728delinsGATGCAGT , CM000672.2:g.43119721_43119728delinsGATGCAGT	GRCh38
NC_000010.10:g.43615169_43615176delinsGATGCAGT , CM000672.1:g.43615169_43615176delinsGATGCAGT	GRCh37
NC_000010.9:g.42935175_42935182delinsGATGCAGT	NCBI36
NG_007489.1:g.47653_47660delinsGATGCAGT , LRG_518:g.47653_47660delinsGATGCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2187_2194delinsGATGCAGT	ENSP00000480088.2:p.Gly729=
ENST00000683007.1:n.2157_2164delinsGATGCAGT
ENST00000683872.1:n.2148_2155delinsGATGCAGT
ENST00000340058.6:c.2583_2590delinsGATGCAGT	ENSP00000344798.4:p.Gly861=
ENST00000355710.8:c.2583_2590delinsGATGCAGT MANE Select	ENSP00000347942.3:p.Gly861=
ENST00000671844.1:c.*1177_*1184delinsGATGCAGT	ENSP00000500541.1:n.*1177_*1184delinsGATGCAGT
ENST00000672389.1:c.*1177_*1184delinsGATGCAGT	ENSP00000500252.1:n.*1177_*1184delinsGATGCAGT
ENST00000340058.5:c.2583_2590delinsGATGCAGT	ENSP00000344798.4:p.Gly861=
ENST00000355710.7:c.2583_2590delinsGATGCAGT	ENSP00000347942.3:p.Gly861=
ENST00000615310.4:c.1309_1316delinsGATGCAGT	ENSP00000480088.1:p.Asp437=
NM_020630.4:c.2583_2590delinsGATGCAGT , LRG_518t2:c.2583_2590delinsGATGCAGT	NP_065681.1:p.Gly861=
NM_020975.4:c.2583_2590delinsGATGCAGT , LRG_518t1:c.2583_2590delinsGATGCAGT	NP_066124.1:p.Gly861=
XM_011540027.1:c.2583_2590delinsGATGCAGT	XP_011538329.1:p.Gly861=
NM_001355216.1:c.1821_1828delinsGATGCAGT	NP_001342145.1:p.Gly607=
NM_020630.5:c.2583_2590delinsGATGCAGT	NP_065681.1:p.Gly861=
NM_020975.5:c.2583_2590delinsGATGCAGT	NP_066124.1:p.Gly861=
NM_020975.6:c.2583_2590delinsGATGCAGT MANE Select	NP_066124.1:p.Gly861=
NM_020630.6:c.2583_2590delinsGATGCAGT	NP_065681.1:p.Gly861=