Canonical Allele Identifier: CA469490672

Gene: RET

Linked Data

• ClinVar Variation Id: 543769
• ClinVar RCV Id: RCV000729527 ; RCV001015327 ; RCV001088057
• dbSNP Id: rs1554817395
• gnomAD v4: 10-43100622-G-T
• MyVariant Identifiers: chr10:g.43596070G>T (hg19) ; chr10:g.43100622G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100622G>T , CM000672.2:g.43100622G>T	GRCh38
NC_000010.10:g.43596070G>T , CM000672.1:g.43596070G>T	GRCh37
NC_000010.9:g.42916076G>T	NCBI36
NG_007489.1:g.28554G>T , LRG_518:g.28554G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.237G>T	ENSP00000480088.2:p.Arg79=
ENST00000683278.1:c.139G>T
ENST00000684216.1:c.139G>T
ENST00000340058.6:c.237G>T	ENSP00000344798.4:p.Arg79=
ENST00000355710.8:c.237G>T MANE Select	ENSP00000347942.3:p.Arg79=
ENST00000638465.1:c.139G>T
ENST00000640619.1:c.139G>T
ENST00000671844.1:c.237G>T	ENSP00000500541.1:p.Arg79=
ENST00000672389.1:c.74-10585G>T	ENSP00000500252.1:n.74-10585G>T
ENST00000340058.5:c.237G>T	ENSP00000344798.4:p.Arg79=
ENST00000355710.7:c.237G>T	ENSP00000347942.3:p.Arg79=
ENST00000498820.5:c.74-11477G>T	ENSP00000419080.1:n.74-11477G>T
ENST00000615310.4:c.237G>T	ENSP00000480088.1:p.Arg79=
NM_020630.4:c.237G>T , LRG_518t2:c.237G>T	NP_065681.1:p.Arg79=
NM_020975.4:c.237G>T , LRG_518t1:c.237G>T	NP_066124.1:p.Arg79=
XM_011540027.1:c.237G>T	XP_011538329.1:p.Arg79=
NM_020630.5:c.237G>T	NP_065681.1:p.Arg79=
NM_020975.5:c.237G>T	NP_066124.1:p.Arg79=
NM_020975.6:c.237G>T MANE Select	NP_066124.1:p.Arg79=
NM_020630.6:c.237G>T	NP_065681.1:p.Arg79=