Canonical Allele Identifier: CA376556992

Gene: RET

Linked Data

• ClinVar Variation Id: 2443064
• ClinVar RCV Id: RCV003274351 ; RCV003150912
• COSMIC: COSM225294
• MyVariant Identifiers: chr10:g.43615538C>T (hg19) ; chr10:g.43120090C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120090C>T , CM000672.2:g.43120090C>T	GRCh38
NC_000010.10:g.43615538C>T , CM000672.1:g.43615538C>T	GRCh37
NC_000010.9:g.42935544C>T	NCBI36
NG_007489.1:g.48022C>T , LRG_518:g.48022C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2221C>T	ENSP00000480088.2:p.Arg741Trp
ENST00000683007.1:n.2191C>T
ENST00000683872.1:n.2182C>T
ENST00000340058.6:c.2617C>T	ENSP00000344798.4:p.Arg873Trp
ENST00000355710.8:c.2617C>T MANE Select	ENSP00000347942.3:p.Arg873Trp
ENST00000671844.1:c.*1211C>T	ENSP00000500541.1:n.*1211C>T
ENST00000672389.1:c.*1211C>T	ENSP00000500252.1:n.*1211C>T
ENST00000340058.5:c.2617C>T	ENSP00000344798.4:p.Arg873Trp
ENST00000355710.7:c.2617C>T	ENSP00000347942.3:p.Arg873Trp
ENST00000615310.4:c.1343C>T	ENSP00000480088.1:p.Ser448Leu
NM_020630.4:c.2617C>T , LRG_518t2:c.2617C>T	NP_065681.1:p.Arg873Trp
NM_020975.4:c.2617C>T , LRG_518t1:c.2617C>T	NP_066124.1:p.Arg873Trp
XM_011540027.1:c.2617C>T	XP_011538329.1:p.Arg873Trp
NM_001355216.1:c.1855C>T	NP_001342145.1:p.Arg619Trp
NM_020630.5:c.2617C>T	NP_065681.1:p.Arg873Trp
NM_020975.5:c.2617C>T	NP_066124.1:p.Arg873Trp
NM_020975.6:c.2617C>T MANE Select	NP_066124.1:p.Arg873Trp
NM_020630.6:c.2617C>T	NP_065681.1:p.Arg873Trp