Canonical Allele Identifier: CA469479767

Gene: RET

Linked Data

• ClinVar Variation Id: 2454150
• ClinVar RCV Id: RCV003172682
• dbSNP Id: rs2132848081
• gnomAD v4: 10-43114571-C-T
• MyVariant Identifiers: chr10:g.43610019C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114571C>T , CM000672.2:g.43114571C>T	GRCh38
NC_000010.10:g.43610019C>T , CM000672.1:g.43610019C>T	GRCh37
NC_000010.9:g.42930025C>T	NCBI36
NG_007489.1:g.42503C>T , LRG_518:g.42503C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1575C>T	ENSP00000480088.2:p.Ile525=
ENST00000683007.1:n.1545C>T
ENST00000683872.1:n.1536C>T
ENST00000340058.6:c.1971C>T	ENSP00000344798.4:p.Ile657=
ENST00000355710.8:c.1971C>T MANE Select	ENSP00000347942.3:p.Ile657=
ENST00000671844.1:c.*565C>T	ENSP00000500541.1:n.*565C>T
ENST00000672389.1:c.*565C>T	ENSP00000500252.1:n.*565C>T
ENST00000340058.5:c.1971C>T	ENSP00000344798.4:p.Ile657=
ENST00000355710.7:c.1971C>T	ENSP00000347942.3:p.Ile657=
ENST00000498820.5:c.522C>T	ENSP00000419080.1:p.Ile174=
ENST00000615310.4:c.1289+3339C>T	ENSP00000480088.1:n.1289+3339C>T
NM_020630.4:c.1971C>T , LRG_518t2:c.1971C>T	NP_065681.1:p.Ile657=
NM_020975.4:c.1971C>T , LRG_518t1:c.1971C>T	NP_066124.1:p.Ile657=
XM_011540027.1:c.1971C>T	XP_011538329.1:p.Ile657=
NM_001355216.1:c.1209C>T	NP_001342145.1:p.Ile403=
NM_020630.5:c.1971C>T	NP_065681.1:p.Ile657=
NM_020975.5:c.1971C>T	NP_066124.1:p.Ile657=
NM_020975.6:c.1971C>T MANE Select	NP_066124.1:p.Ile657=
NM_020630.6:c.1971C>T	NP_065681.1:p.Ile657=