Canonical Allele Identifier: CA469479772

Gene: RET

Linked Data

• ClinVar Variation Id: 1783674
• ClinVar RCV Id: RCV002423546
• dbSNP Id: rs779310191
• MyVariant Identifiers: chr10:g.43610022C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114574C>T , CM000672.2:g.43114574C>T	GRCh38
NC_000010.10:g.43610022C>T , CM000672.1:g.43610022C>T	GRCh37
NC_000010.9:g.42930028C>T	NCBI36
NG_007489.1:g.42506C>T , LRG_518:g.42506C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1578C>T	ENSP00000480088.2:p.His526=
ENST00000683007.1:n.1548C>T
ENST00000683872.1:n.1539C>T
ENST00000340058.6:c.1974C>T	ENSP00000344798.4:p.His658=
ENST00000355710.8:c.1974C>T MANE Select	ENSP00000347942.3:p.His658=
ENST00000671844.1:c.*568C>T	ENSP00000500541.1:n.*568C>T
ENST00000672389.1:c.*568C>T	ENSP00000500252.1:n.*568C>T
ENST00000340058.5:c.1974C>T	ENSP00000344798.4:p.His658=
ENST00000355710.7:c.1974C>T	ENSP00000347942.3:p.His658=
ENST00000498820.5:c.525C>T	ENSP00000419080.1:p.His175=
ENST00000615310.4:c.1289+3342C>T	ENSP00000480088.1:n.1289+3342C>T
NM_020630.4:c.1974C>T , LRG_518t2:c.1974C>T	NP_065681.1:p.His658=
NM_020975.4:c.1974C>T , LRG_518t1:c.1974C>T	NP_066124.1:p.His658=
XM_011540027.1:c.1974C>T	XP_011538329.1:p.His658=
NM_001355216.1:c.1212C>T	NP_001342145.1:p.His404=
NM_020630.5:c.1974C>T	NP_065681.1:p.His658=
NM_020975.5:c.1974C>T	NP_066124.1:p.His658=
NM_020975.6:c.1974C>T MANE Select	NP_066124.1:p.His658=
NM_020630.6:c.1974C>T	NP_065681.1:p.His658=