Canonical Allele Identifier: CA035484

Gene: RET

Linked Data

• ClinVar Variation Id: 1611774
• ClinVar RCV Id: RCV002148242
• dbSNP Id: rs766839936
• ExAC: 10:43608984 T / C
• gnomAD v2: 10-43608984-T-C
• gnomAD v3: 10-43113536-T-C
• gnomAD v4: 10-43113536-T-C
• MyVariant Identifiers: chr10:g.43608984T>C (hg19) ; chr10:g.43113536T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113536T>C , CM000672.2:g.43113536T>C	GRCh38
NC_000010.10:g.43608984T>C , CM000672.1:g.43608984T>C	GRCh37
NC_000010.9:g.42928990T>C	NCBI36
NG_007489.1:g.41468T>C , LRG_518:g.41468T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1364-20T>C	ENSP00000480088.2:n.1364-20T>C
ENST00000683007.1:n.1334-20T>C
ENST00000683872.1:n.521-20T>C
ENST00000340058.6:c.1760-20T>C	ENSP00000344798.4:n.1760-20T>C
ENST00000355710.8:c.1760-20T>C MANE Select	ENSP00000347942.3:n.1760-20T>C
ENST00000671844.1:c.*354-20T>C	ENSP00000500541.1:n.*354-20T>C
ENST00000672389.1:c.*354-20T>C	ENSP00000500252.1:n.*354-20T>C
ENST00000340058.5:c.1760-20T>C	ENSP00000344798.4:n.1760-20T>C
ENST00000355710.7:c.1760-20T>C	ENSP00000347942.3:n.1760-20T>C
ENST00000498820.5:c.311-20T>C	ENSP00000419080.1:n.311-20T>C
ENST00000615310.4:c.1289+2304T>C	ENSP00000480088.1:n.1289+2304T>C
NM_020630.4:c.1760-20T>C , LRG_518t2:c.1760-20T>C	NP_065681.1:n.1760-20T>C
NM_020975.4:c.1760-20T>C , LRG_518t1:c.1760-20T>C	NP_066124.1:n.1760-20T>C
XM_011540027.1:c.1760-20T>C	XP_011538329.1:n.1760-20T>C
NM_001355216.1:c.998-20T>C	NP_001342145.1:n.998-20T>C
NM_020630.5:c.1760-20T>C	NP_065681.1:n.1760-20T>C
NM_020975.5:c.1760-20T>C	NP_066124.1:n.1760-20T>C
NM_020975.6:c.1760-20T>C MANE Select	NP_066124.1:n.1760-20T>C
NM_020630.6:c.1760-20T>C	NP_065681.1:n.1760-20T>C