Canonical Allele Identifier: CA2608875675

Gene: RET

Linked Data

• gnomAD v4: 10-43119860-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119862_43119863del , CM000672.2:g.43119862_43119863del	GRCh38
NC_000010.10:g.43615310_43615311del , CM000672.1:g.43615310_43615311del	GRCh37
NC_000010.9:g.42935316_42935317del	NCBI36
NG_007489.1:g.47794_47795del , LRG_518:g.47794_47795del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+117_2211+118del	ENSP00000480088.2:n.2211+117_2211+118del
ENST00000683007.1:n.2181+117_2181+118del
ENST00000683872.1:n.2172+117_2172+118del
ENST00000340058.6:c.2607+117_2607+118del	ENSP00000344798.4:n.2607+117_2607+118del
ENST00000355710.8:c.2607+117_2607+118del MANE Select	ENSP00000347942.3:n.2607+117_2607+118del
ENST00000671844.1:c.*1201+117_*1201+118del	ENSP00000500541.1:n.*1201+117_*1201+118del
ENST00000672389.1:c.*1201+117_*1201+118del	ENSP00000500252.1:n.*1201+117_*1201+118del
ENST00000340058.5:c.2607+117_2607+118del	ENSP00000344798.4:n.2607+117_2607+118del
ENST00000355710.7:c.2607+117_2607+118del	ENSP00000347942.3:n.2607+117_2607+118del
ENST00000615310.4:c.1333+117_1333+118del	ENSP00000480088.1:n.1333+117_1333+118del
NM_020630.4:c.2607+117_2607+118del , LRG_518t2:c.2607+117_2607+118del	NP_065681.1:n.2607+117_2607+118del
NM_020975.4:c.2607+117_2607+118del , LRG_518t1:c.2607+117_2607+118del	NP_066124.1:n.2607+117_2607+118del
XM_011540027.1:c.2607+117_2607+118del	XP_011538329.1:n.2607+117_2607+118del
NM_001355216.1:c.1845+117_1845+118del	NP_001342145.1:n.1845+117_1845+118del
NM_020630.5:c.2607+117_2607+118del	NP_065681.1:n.2607+117_2607+118del
NM_020975.5:c.2607+117_2607+118del	NP_066124.1:n.2607+117_2607+118del
NM_020975.6:c.2607+117_2607+118del MANE Select	NP_066124.1:n.2607+117_2607+118del
NM_020630.6:c.2607+117_2607+118del	NP_065681.1:n.2607+117_2607+118del