Canonical Allele Identifier: CA10628534

Gene: RET

Linked Data

• ClinVar Variation Id: 299885
• ClinVar RCV Id: RCV000298833 ; RCV000336868 ; RCV000369892 ; RCV000393831 ; RCV002256191
• dbSNP Id: rs886046985
• gnomAD v2: 10-43572575-G-T
• gnomAD v3: 10-43077127-G-T
• gnomAD v4: 10-43077127-G-T
• MyVariant Identifiers: chr10:g.43572575G>T (hg19) ; chr10:g.43077127G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077127G>T , CM000672.2:g.43077127G>T	GRCh38
NC_000010.10:g.43572575G>T , CM000672.1:g.43572575G>T	GRCh37
NC_000010.9:g.42892581G>T	NCBI36
NG_007489.1:g.5059G>T , LRG_518:g.5059G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.-132G>T	ENSP00000480088.2:n.-132G>T
ENST00000340058.6:c.-132G>T	ENSP00000344798.4:n.-132G>T
ENST00000355710.8:c.-132G>T MANE Select	ENSP00000347942.3:n.-132G>T
ENST00000671844.1:c.-132G>T	ENSP00000500541.1:n.-132G>T
ENST00000672389.1:c.-132G>T	ENSP00000500252.1:n.-132G>T
ENST00000340058.5:c.-132G>T	ENSP00000344798.4:n.-132G>T
ENST00000355710.7:c.-132G>T	ENSP00000347942.3:n.-132G>T
ENST00000498820.5:c.-132G>T	ENSP00000419080.1:n.-132G>T
ENST00000615310.4:c.-132G>T	ENSP00000480088.1:n.-132G>T
NM_020630.4:c.-132G>T , LRG_518t2:c.-132G>T	NP_065681.1:n.-132G>T
NM_020975.4:c.-132G>T , LRG_518t1:c.-132G>T	NP_066124.1:n.-132G>T
XM_011540027.1:c.-132G>T	XP_011538329.1:n.-132G>T
NM_020630.5:c.-132G>T	NP_065681.1:n.-132G>T
NM_020975.5:c.-132G>T	NP_066124.1:n.-132G>T
NM_020975.6:c.-132G>T MANE Select	NP_066124.1:n.-132G>T
NM_020630.6:c.-132G>T	NP_065681.1:n.-132G>T