Canonical Allele Identifier: CA593292882

Gene: RET

Linked Data

• ClinVar Variation Id: 1653287
• ClinVar RCV Id: RCV002161011
• dbSNP Id: rs1453857349
• gnomAD v2: 10-43595895-T-TAC
• gnomAD v3: 10-43100447-T-TAC
• gnomAD v4: 10-43100447-T-TAC
• MyVariant Identifiers: chr10:g.43595895_43595896insAC (hg19) ; chr10:g.43100447_43100448insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100448_43100449dup , CM000672.2:g.43100448_43100449dup	GRCh38
NC_000010.10:g.43595896_43595897dup , CM000672.1:g.43595896_43595897dup	GRCh37
NC_000010.9:g.42915902_42915903dup	NCBI36
NG_007489.1:g.28380_28381dup , LRG_518:g.28380_28381dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.74-11_74-10dup	ENSP00000480088.2:n.74-11_74-10dup
ENST00000340058.6:c.74-11_74-10dup	ENSP00000344798.4:n.74-11_74-10dup
ENST00000355710.8:c.74-11_74-10dup MANE Select	ENSP00000347942.3:n.74-11_74-10dup
ENST00000671844.1:c.74-11_74-10dup	ENSP00000500541.1:n.74-11_74-10dup
ENST00000672389.1:c.74-10759_74-10758dup	ENSP00000500252.1:n.74-10759_74-10758dup
ENST00000340058.5:c.74-11_74-10dup	ENSP00000344798.4:n.74-11_74-10dup
ENST00000355710.7:c.74-11_74-10dup	ENSP00000347942.3:n.74-11_74-10dup
ENST00000498820.5:c.74-11651_74-11650dup	ENSP00000419080.1:n.74-11651_74-11650dup
ENST00000615310.4:c.74-11_74-10dup	ENSP00000480088.1:n.74-11_74-10dup
NM_020630.4:c.74-11_74-10dup , LRG_518t2:c.74-11_74-10dup	NP_065681.1:n.74-11_74-10dup
NM_020975.4:c.74-11_74-10dup , LRG_518t1:c.74-11_74-10dup	NP_066124.1:n.74-11_74-10dup
XM_011540027.1:c.74-11_74-10dup	XP_011538329.1:n.74-11_74-10dup
NM_020630.5:c.74-11_74-10dup	NP_065681.1:n.74-11_74-10dup
NM_020975.5:c.74-11_74-10dup	NP_066124.1:n.74-11_74-10dup
NM_020975.6:c.74-11_74-10dup MANE Select	NP_066124.1:n.74-11_74-10dup
NM_020630.6:c.74-11_74-10dup	NP_065681.1:n.74-11_74-10dup