Canonical Allele Identifier: CA665316898

Gene: RET

Linked Data

• dbSNP Id: rs1470788618
• gnomAD v4: 10-43114412-T-C
• MyVariant Identifiers: chr10:g.43609860T>C (hg19) ; chr10:g.43114412T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114412T>C , CM000672.2:g.43114412T>C	GRCh38
NC_000010.10:g.43609860T>C , CM000672.1:g.43609860T>C	GRCh37
NC_000010.9:g.42929866T>C	NCBI36
NG_007489.1:g.42344T>C , LRG_518:g.42344T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1484-68T>C	ENSP00000480088.2:n.1484-68T>C
ENST00000683007.1:n.1454-68T>C
ENST00000683872.1:n.1377T>C
ENST00000340058.6:c.1880-68T>C	ENSP00000344798.4:n.1880-68T>C
ENST00000355710.8:c.1880-68T>C MANE Select	ENSP00000347942.3:n.1880-68T>C
ENST00000671844.1:c.*474-68T>C	ENSP00000500541.1:n.*474-68T>C
ENST00000672389.1:c.*474-68T>C	ENSP00000500252.1:n.*474-68T>C
ENST00000340058.5:c.1880-68T>C	ENSP00000344798.4:n.1880-68T>C
ENST00000355710.7:c.1880-68T>C	ENSP00000347942.3:n.1880-68T>C
ENST00000498820.5:c.431-68T>C	ENSP00000419080.1:n.431-68T>C
ENST00000615310.4:c.1289+3180T>C	ENSP00000480088.1:n.1289+3180T>C
NM_020630.4:c.1880-68T>C , LRG_518t2:c.1880-68T>C	NP_065681.1:n.1880-68T>C
NM_020975.4:c.1880-68T>C , LRG_518t1:c.1880-68T>C	NP_066124.1:n.1880-68T>C
XM_011540027.1:c.1880-68T>C	XP_011538329.1:n.1880-68T>C
NM_001355216.1:c.1118-68T>C	NP_001342145.1:n.1118-68T>C
NM_020630.5:c.1880-68T>C	NP_065681.1:n.1880-68T>C
NM_020975.5:c.1880-68T>C	NP_066124.1:n.1880-68T>C
NM_020975.6:c.1880-68T>C MANE Select	NP_066124.1:n.1880-68T>C
NM_020630.6:c.1880-68T>C	NP_065681.1:n.1880-68T>C