Canonical Allele Identifier: CA469479598

Gene: RET

Linked Data

• ClinVar Variation Id: 3227517
• ClinVar RCV Id: RCV004524635
• dbSNP Id: rs761187737
• gnomAD v4: 10-43114511-G-A
• MyVariant Identifiers: chr10:g.43609959G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114511G>A , CM000672.2:g.43114511G>A	GRCh38
NC_000010.10:g.43609959G>A , CM000672.1:g.43609959G>A	GRCh37
NC_000010.9:g.42929965G>A	NCBI36
NG_007489.1:g.42443G>A , LRG_518:g.42443G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1515G>A	ENSP00000480088.2:p.Val505=
ENST00000683007.1:n.1485G>A
ENST00000683872.1:n.1476G>A
ENST00000340058.6:c.1911G>A	ENSP00000344798.4:p.Val637=
ENST00000355710.8:c.1911G>A MANE Select	ENSP00000347942.3:p.Val637=
ENST00000671844.1:c.*505G>A	ENSP00000500541.1:n.*505G>A
ENST00000672389.1:c.*505G>A	ENSP00000500252.1:n.*505G>A
ENST00000340058.5:c.1911G>A	ENSP00000344798.4:p.Val637=
ENST00000355710.7:c.1911G>A	ENSP00000347942.3:p.Val637=
ENST00000498820.5:c.462G>A	ENSP00000419080.1:p.Val154=
ENST00000615310.4:c.1289+3279G>A	ENSP00000480088.1:n.1289+3279G>A
NM_020630.4:c.1911G>A , LRG_518t2:c.1911G>A	NP_065681.1:p.Val637=
NM_020975.4:c.1911G>A , LRG_518t1:c.1911G>A	NP_066124.1:p.Val637=
XM_011540027.1:c.1911G>A	XP_011538329.1:p.Val637=
NM_001355216.1:c.1149G>A	NP_001342145.1:p.Val383=
NM_020630.5:c.1911G>A	NP_065681.1:p.Val637=
NM_020975.5:c.1911G>A	NP_066124.1:p.Val637=
NM_020975.6:c.1911G>A MANE Select	NP_066124.1:p.Val637=
NM_020630.6:c.1911G>A	NP_065681.1:p.Val637=