Canonical Allele Identifier: CA915945893

Gene: RET

Linked Data

• ClinVar Variation Id: 792378
• ClinVar RCV Id: RCV000975473
• dbSNP Id: rs1588848600
• gnomAD v4: 10-43077339-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077340del , CM000672.2:g.43077340del	GRCh38
NC_000010.10:g.43572788del , CM000672.1:g.43572788del	GRCh37
NC_000010.9:g.42892794del	NCBI36
NG_007489.1:g.5272del , LRG_518:g.5272del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.73+9del	ENSP00000480088.2:n.73+9del
ENST00000340058.6:c.73+9del	ENSP00000344798.4:n.73+9del
ENST00000355710.8:c.73+9del MANE Select	ENSP00000347942.3:n.73+9del
ENST00000671844.1:c.73+9del	ENSP00000500541.1:n.73+9del
ENST00000672389.1:c.73+9del	ENSP00000500252.1:n.73+9del
ENST00000340058.5:c.73+9del	ENSP00000344798.4:n.73+9del
ENST00000355710.7:c.73+9del	ENSP00000347942.3:n.73+9del
ENST00000498820.5:c.73+9del	ENSP00000419080.1:n.73+9del
ENST00000615310.4:c.73+9del	ENSP00000480088.1:n.73+9del
NM_020630.4:c.73+9del , LRG_518t2:c.73+9del	NP_065681.1:n.73+9del
NM_020975.4:c.73+9del , LRG_518t1:c.73+9del	NP_066124.1:n.73+9del
XM_011540027.1:c.73+9del	XP_011538329.1:n.73+9del
NM_020630.5:c.73+9del	NP_065681.1:n.73+9del
NM_020975.5:c.73+9del	NP_066124.1:n.73+9del
NM_020975.6:c.73+9del MANE Select	NP_066124.1:n.73+9del
NM_020630.6:c.73+9del	NP_065681.1:n.73+9del