Canonical Allele Identifier: CA2608894489

Gene: RET

Linked Data

• gnomAD v4: 10-43077311-TGCTGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077317_43077322del , CM000672.2:g.43077317_43077322del	GRCh38
NC_000010.10:g.43572765_43572770del , CM000672.1:g.43572765_43572770del	GRCh37
NC_000010.9:g.42892771_42892776del	NCBI36
NG_007489.1:g.5249_5254del , LRG_518:g.5249_5254del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.59_64del	ENSP00000480088.2:p.Pro20_Leu21del
ENST00000340058.6:c.59_64del	ENSP00000344798.4:p.Pro20_Leu21del
ENST00000355710.8:c.59_64del MANE Select	ENSP00000347942.3:p.Pro20_Leu21del
ENST00000671844.1:c.59_64del	ENSP00000500541.1:p.Pro20_Leu21del
ENST00000672389.1:c.59_64del	ENSP00000500252.1:p.Pro20_Leu21del
ENST00000340058.5:c.59_64del	ENSP00000344798.4:p.Pro20_Leu21del
ENST00000355710.7:c.59_64del	ENSP00000347942.3:p.Pro20_Leu21del
ENST00000498820.5:c.59_64del	ENSP00000419080.1:p.Pro20_Leu21del
ENST00000615310.4:c.59_64del	ENSP00000480088.1:p.Pro20_Leu21del
NM_020630.4:c.59_64del , LRG_518t2:c.59_64del	NP_065681.1:p.Pro20_Leu21del
NM_020975.4:c.59_64del , LRG_518t1:c.59_64del	NP_066124.1:p.Pro20_Leu21del
XM_011540027.1:c.59_64del	XP_011538329.1:p.Pro20_Leu21del
NM_020630.5:c.59_64del	NP_065681.1:p.Pro20_Leu21del
NM_020975.5:c.59_64del	NP_066124.1:p.Pro20_Leu21del
NM_020975.6:c.59_64del MANE Select	NP_066124.1:p.Pro20_Leu21del
NM_020630.6:c.59_64del	NP_065681.1:p.Pro20_Leu21del