Canonical Allele Identifier: CA043526

Gene: RET

Linked Data

• ClinVar Variation Id: 477374
• ClinVar RCV Id: RCV000526991 ; RCV002225663
• dbSNP Id: rs751005619
• ExAC: 10:43572670 G / C
• gnomAD v2: 10-43572670-G-C
• gnomAD v3: 10-43077222-G-C
• gnomAD v4: 10-43077222-G-C
• MyVariant Identifiers: chr10:g.43572670G>C (hg19) ; chr10:g.43077222G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077222G>C , CM000672.2:g.43077222G>C	GRCh38
NC_000010.10:g.43572670G>C , CM000672.1:g.43572670G>C	GRCh37
NC_000010.9:g.42892676G>C	NCBI36
NG_007489.1:g.5154G>C , LRG_518:g.5154G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.-37G>C	ENSP00000480088.2:n.-37G>C
ENST00000340058.6:c.-37G>C	ENSP00000344798.4:n.-37G>C
ENST00000355710.8:c.-37G>C MANE Select	ENSP00000347942.3:n.-37G>C
ENST00000671844.1:c.-37G>C	ENSP00000500541.1:n.-37G>C
ENST00000672389.1:c.-37G>C	ENSP00000500252.1:n.-37G>C
ENST00000340058.5:c.-37G>C	ENSP00000344798.4:n.-37G>C
ENST00000355710.7:c.-37G>C	ENSP00000347942.3:n.-37G>C
ENST00000498820.5:c.-37G>C	ENSP00000419080.1:n.-37G>C
ENST00000615310.4:c.-37G>C	ENSP00000480088.1:n.-37G>C
NM_020630.4:c.-37G>C , LRG_518t2:c.-37G>C	NP_065681.1:n.-37G>C
NM_020975.4:c.-37G>C , LRG_518t1:c.-37G>C	NP_066124.1:n.-37G>C
XM_011540027.1:c.-37G>C	XP_011538329.1:n.-37G>C
NM_020630.5:c.-37G>C	NP_065681.1:n.-37G>C
NM_020975.5:c.-37G>C	NP_066124.1:n.-37G>C
NM_020975.6:c.-37G>C MANE Select	NP_066124.1:n.-37G>C
NM_020630.6:c.-37G>C	NP_065681.1:n.-37G>C