Canonical Allele Identifier: CA2608869615

Gene: RET

Linked Data

• gnomAD v4: 10-43106277-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106280del , CM000672.2:g.43106280del	GRCh38
NC_000010.10:g.43601728del , CM000672.1:g.43601728del	GRCh37
NC_000010.9:g.42921734del	NCBI36
NG_007489.1:g.34212del , LRG_518:g.34212del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.867+1087del	ENSP00000480088.2:n.867+1087del
ENST00000683007.1:n.442-96del
ENST00000340058.6:c.868-96del	ENSP00000344798.4:n.868-96del
ENST00000355710.8:c.868-96del MANE Select	ENSP00000347942.3:n.868-96del
ENST00000671844.1:c.625+3651del	ENSP00000500541.1:n.625+3651del
ENST00000672389.1:c.74-4927del	ENSP00000500252.1:n.74-4927del
ENST00000340058.5:c.868-96del	ENSP00000344798.4:n.868-96del
ENST00000355710.7:c.868-96del	ENSP00000347942.3:n.868-96del
ENST00000479913.1:n.463-96del
ENST00000498820.5:c.74-5819del	ENSP00000419080.1:n.74-5819del
ENST00000615310.4:c.868-96del	ENSP00000480088.1:n.868-96del
NM_020630.4:c.868-96del , LRG_518t2:c.868-96del	NP_065681.1:n.868-96del
NM_020975.4:c.868-96del , LRG_518t1:c.868-96del	NP_066124.1:n.868-96del
XM_011540027.1:c.868-96del	XP_011538329.1:n.868-96del
NM_001355216.1:c.106-96del	NP_001342145.1:n.106-96del
NM_020630.5:c.868-96del	NP_065681.1:n.868-96del
NM_020975.5:c.868-96del	NP_066124.1:n.868-96del
NM_020975.6:c.868-96del MANE Select	NP_066124.1:n.868-96del
NM_020630.6:c.868-96del	NP_065681.1:n.868-96del