Canonical Allele Identifier: CA1905819524

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119775_43119776delinsGC , CM000672.2:g.43119775_43119776delinsGC	GRCh38
NC_000010.10:g.43615223_43615224delinsGC , CM000672.1:g.43615223_43615224delinsGC	GRCh37
NC_000010.9:g.42935229_42935230delinsGC	NCBI36
NG_007489.1:g.47707_47708delinsGC , LRG_518:g.47707_47708delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+30_2211+31delinsGC	ENSP00000480088.2:n.2211+30_2211+31delinsGC
ENST00000683007.1:n.2181+30_2181+31delinsGC
ENST00000683872.1:n.2172+30_2172+31delinsGC
ENST00000340058.6:c.2607+30_2607+31delinsGC	ENSP00000344798.4:n.2607+30_2607+31delinsGC
ENST00000355710.8:c.2607+30_2607+31delinsGC MANE Select	ENSP00000347942.3:n.2607+30_2607+31delinsGC
ENST00000671844.1:c.*1201+30_*1201+31delinsGC	ENSP00000500541.1:n.*1201+30_*1201+31delinsGC
ENST00000672389.1:c.*1201+30_*1201+31delinsGC	ENSP00000500252.1:n.*1201+30_*1201+31delinsGC
ENST00000340058.5:c.2607+30_2607+31delinsGC	ENSP00000344798.4:n.2607+30_2607+31delinsGC
ENST00000355710.7:c.2607+30_2607+31delinsGC	ENSP00000347942.3:n.2607+30_2607+31delinsGC
ENST00000615310.4:c.1333+30_1333+31delinsGC	ENSP00000480088.1:n.1333+30_1333+31delinsGC
NM_020630.4:c.2607+30_2607+31delinsGC , LRG_518t2:c.2607+30_2607+31delinsGC	NP_065681.1:n.2607+30_2607+31delinsGC
NM_020975.4:c.2607+30_2607+31delinsGC , LRG_518t1:c.2607+30_2607+31delinsGC	NP_066124.1:n.2607+30_2607+31delinsGC
XM_011540027.1:c.2607+30_2607+31delinsGC	XP_011538329.1:n.2607+30_2607+31delinsGC
NM_001355216.1:c.1845+30_1845+31delinsGC	NP_001342145.1:n.1845+30_1845+31delinsGC
NM_020630.5:c.2607+30_2607+31delinsGC	NP_065681.1:n.2607+30_2607+31delinsGC
NM_020975.5:c.2607+30_2607+31delinsGC	NP_066124.1:n.2607+30_2607+31delinsGC
NM_020975.6:c.2607+30_2607+31delinsGC MANE Select	NP_066124.1:n.2607+30_2607+31delinsGC
NM_020630.6:c.2607+30_2607+31delinsGC	NP_065681.1:n.2607+30_2607+31delinsGC